Protection against mycobacterial infections

ABSTRACT

The present invention relates to a method of identifying mycobacterial genes which were induced or up-regulated during  M. tuberculosis  virulence, and to isolated peptide products of said genes. Also provided, are inhibitors of said genes, and antibodies which bind to said peptide products. Further embodiments include DNA and RNA vectors encoding said products, attenuated mycobacteria in which the activity of at least one of said genes or peptide products has been modified, vaccines against mycobacterial infections, and methods of detecting a mycobacterial infection.

[0001] The present invention relates to a method of identifying mycobacterial genes which are induced or up-regulated during mycobacterial virulence, to isolated peptide products of said genes, to inhibitors of said genes, to antibodies which bind to said peptide products, to DNA and RNA vectors encoding said products, to attenuated mycobacteria in which the activity of at least one of said genes or peptide products has been modified, to vaccines against mycobacterial infections, and to methods of detecting a mycobacterial infection.

[0002] Many microorganisms are capable of forming intracellular infections. These include: infections caused by species of Salmonella, Yersinia, Shigella, Campylobacter, Chlamydia and Mycobacteria. Some of these infections are exclusively intracellular, others contain both intracellular and extracellular components. However, it is the intracellular survival cycle of bacterial infection which is suspected as a main supportive factor for disease progression.

[0003] Generally, these microorganisms do not circulate freely in the body, for example, in the bloodstream, and are often not amenable to drug treatment regimes. Where drugs are available, this problem has been exacerbated by the development of multiple drug resistant microorganisms.

[0004] A number of factors have contributed to the problem of microbial drug resistance. One is the accumulation of mutations over time and the subsequent horizontal and vertical transfer of the mutated genes to other organisms. Thus, for a given pathogen, entire classes of antibiotics have been rendered inactive. A further factor has been the absence of a new class of antibiotics in recent years. The emergence of multiple drug-resistant pathogenic bacteria represents a serious threat to public health and new forms of therapy are urgently required.

[0005] For similar reasons, vaccine therapies have not proved effective against such intracellular microorganisms. Also, increased systemic concentration of antibiotics to improve bioavailability within cells may result in severe side effects.

[0006]Mycobacterium tuberculosis and closely related species make up a small group of mycobacteria known as the Mycobacterium tuberculosis complex (MTC). This group comprises four species M. tuberculosis, M. microti, M. bovis and M. africanum which are the causative agent in the majority of tuberculosis (TB) cases throughout the world.

[0007]M. tuberculosis is responsible for more than three million deaths a year world-wide. Other mycobacteria are also pathogenic in man and animals, for example M. avium subsp. paratuberculosis which causes Johne's disease in ruminants, M. bovis which causes tuberculosis in cattle, M. abvium and M. intracellulare which cause tuberculosis in immunocompromised patients (eg. AIDS patients, and bone marrow transplant patients) and M. leprae which causes leprosy in humans.

[0008]M. tuberculosis infects macrophage cells within the body, particularly alveolar macrophages in the lung. Soon after macrophage infection, most M. tuberculosis bacteria enter, persist and replicate within cellular phagosome vesicles, where the bacteria are sequestered from host defences and extracellular factors.

[0009] It is the intracellular survival and multiplication or replication of bacterial infection which is suspected as a main supportive factor for mycobacterial disease progression.

[0010] A number of drug therapy regimens have been proposed for combatting M. tuberculosis infections, and currently combination therapy including the drug isoniazid has proved most effective. However, one problem with such treatment regimes is that they are long-term, and failure to complete such treatment can promote the development of multiple drug resistant microorganisms.

[0011] A further problem is that of providing an adequate bioavailability of the drug within the cells to be treated. Whilst it is possible to increase the systemic concentration of a drug (eg. by administering a higher dosage) this may result in severe side effects caused by the increased drug concentration.

[0012] The effectiveness of vaccine prevention against M. tuberculosis has varied widely. The current M. tuberculosis vaccine, BCG, is an attenuated strain of M. bovis. It is ,effective against severe complications of TB in children, but it varies greatly in its effectiveness in adults particularly across ethnic groups. BCG vaccination has been used to prevent tuberculous meningitis and helps prevent the spread of M. tuberculosis to extra-pulmonary sites, but does not prevent infection. Furthermore, it can not be administered to immunocompromised individuals, a group particularly susceptible to TB, because of the risk of systemic disease resulting from the vaccine.

[0013] The limited efficacy of BCG and the global prevalence of TB has led to an international effort to generate new, more effective vaccines. The current paradigm is that protection will be mediated by the stimulation of a Th1 immune response.

[0014] BCG vaccination in man was given orally when originally introduced, but that route was discontinued because of loss of viable BCG during gastric passage and of frequent cervical adenopathy. In experimental animal species, aerosol or intra-tracheal delivery of BCG has been achieved without adverse effects, but has varied in efficacy from superior protection than parenteral inoculation in primates, mice and guinea pigs to no apparent advantage over the subcutaneous route in other studies.

[0015] There is therefore a need for an improved and/or alternative vaccine or therapeutic agent for combatting mycobacterial infections.

[0016] This need is addressed by the present invention.

[0017] According to a first aspect, the present invention provides a method of identifying a mycobacterial nucleic acid promoter sequence which, is induced or up-regulated during mycobacterial virulence, said method comprising:

[0018] infecting a macrophage target cell with a Mycobacterium tuberculosis host cell, which host cell contains a nucleic acid construct comprising a putative mycobacterial promoter sequence operably linked to a coding sequence of a reporter gene located down-stream from the promoter;

[0019] culturing the macrophage under conditions which support mycobacterial virulence; and

[0020] identifying a promoter sequence which is induced or up-regulated during virulence by detecting expression of the reporter sequence.

[0021]M. tuberculosis is a high containment pathogen, and use of this microorganism is therefore preferably conducted under Advisory Committee for Dangerous Pathogen (ACDP) 3 conditions.

[0022]M. tuberculosis pursues a route of intracellular infection, and there are several differences in the behaviour of M. tuberculosis compared to other pathogens. Thus, nucleic acid expression profiles of other bacteria during infection, even other mycobacteria, do not accurately reflect the series of changes which occur during M. tuberculosis infection.

[0023] For example, M. tuberculosis does not use type III secretion systems to inject effector molecules to alter host cell behaviour as do Salmonella species nor does it utilise pore forming toxins such as listeriolysin to escape the phagosomal vesicle as found in L. monocytogenes infection.

[0024] Pathogenic mycobacteria appear to rely upon a repertoire of gene products which are tightly regulated in response to the interaction with a host cell, many of which have yet to be identified.

[0025] In comparison with other mycobacterial pathogens, species such as M. leprae and M. marinum appear to have a thermotropism where the infection is manifested in the periphery of the body where temperatures are lower than the typical 37° C. core body temperature. M. leprae also targets the myelin sheath of the nerve cells and the disease pathology reflects this tissue tropism. M. marinum causes a limited infection resulting in a surface lesion on the skin which can be self-limiting. Other pathogens such as M. avium and M. intracellulare typically cause infections in immunocompromised individuals and do not usually have the ability to cause disease in healthy subjects. M. bovis infection is usually acquired through ingestion of contaminated milk products resulting in infection via the lymph nodes and leading to lymphoadenopathy. Following infection, M. tuberculosis may enter a dormant state leading to a latent infection. This latent infection may persist for decades before reactivation occurs leading to progressive active disease.

[0026] Other mycobacterial species may share in common with M. tuberculosis some components of conserved virulence mechanisms. However, with the publication of the genome sequences for M. tuberculosis and M. leprae, and the publication of other partially completed genome sequences (eg. M. smegmatis, and M. bovis), it is clear there are significant differences between the different mycobacterial pathogens that ultimately define their success as pathogens and the characteristics of the pathology of the diseases that they cause.

[0027] Thus, M. tuberculosis is a specialised bacterial pathogen typically spread by inhalation. M. tuberculosis has a complex interaction with its host, from initial contact with host macrophage onwards, which it manipulates to its own advantage leading to either progressive active disease, or a persistent latent infection or most likely a limited infection which is cleared or contained indefinitely by the host.

[0028] Mycobacterial virulence includes one or more of the events associated with infection by a mycobacterium of its natural target cell. For example, a natural target cell of M. tuberculosis is a macrophage, and virulence with respect to this bacterium and target cell would include any event involved during the sequence of events comprising phagocytosis by the macrophage or uptake via alternative pathways of the bacterium, formation of the phagosome, multiplication of the bacterium within the phagosome, lysis of the phagosome/host cell, and spread of the lesion to a secondary site (ie. haematogenous spread). Thus, virulence conditions are culture conditions which are conducive for a mycobacterium to express at least one gene which would be normally expressed in vivo during infection of the mycobacterium's natural target cell.

[0029] In one embodiment, the putative promoter sequence is selected from the species M. phlei, M. smegmatis, M. africanum, M. caneti, M. fortuitum, M. marinum, M. ulcerans, M. tuberculosis, M. bovis, M. microti, M. avium, M. paratuberculosis, M. leprae, M. lepraemurium, M. intracellulare, M. scrofulaceum, M. xenopi, M. genavense, M. kansasii, M. simiae, M. szulgai, M. haemophilum, M. asiaticum, M. malmoense, M. vaccae and M. shimoidei. Of particular interest are members of the MTC, preferably M. tuberculosis or M. bovis.

[0030] In another embodiment, the reporter gene is a silent marker of gene expression, and does not require a selection pressure to be applied during the detection step. This is in contrast to other markers, for example, antibiotic resistance markers which require the presence of the antibiotic to permit selection of desirable transformants. The presence of a selection pressure may be undesirable as this pressure may itself induce or cause up-regulation of other genes, or result in the loss of transiently-expressed promoters. The induction or up-regulation of other genes, eg. growth-related genes, may result in increased growth of background mycobacteria and may cause problems in the identification of desirable transformants free of false positives.

[0031] The reporter sequences employed in the method of the present invention do not possess their own promoters, and are therefore reliant on the activity of the putative promoter sequence to effect expression thereof. Thus, by culturing mycobacterial host cells under virulence conditions, it is possible to select for those promoters which are active under virulence conditions by detecting expression of the reporter sequence.

[0032] The reporter gene is preferably a Green Fluorescent Protein (GFP). Suitable GFPs such as GFPmut 1, 2 or 3 are described in [Cormack et al. (1996) Gene, 173, pp.33-38]. In a preferred embodiment, the GFP is GFPmut2.

[0033] In those embodiments in which the reporter sequence encodes a fluorescent protein, the desirable mycobacterial host cell transformants are capable of fluorescence by expression of the reporter sequence.

[0034] Thus, in a preferred embodiment, promoters active during virulence are detected by differential fluorescence induction methods (DFI) as, for example, described in Valdivia, R. H. and Falkow, S. (1997) [Science, vol. 277, Sep. 26, 1997, pp. 2007-2011], and desirable transformed host cells containing said promoters may be isolated by fluorescence activated cell sorting (FACS).

[0035] In use, the mycobacterial host cell infects a macrophage in vitro. Thereafter, when recovering the mycobacteria (eg. for FACS analysis), phagosomal vesicles containing the bacteria may be recovered and the vesicles analysed (ie. sorted) whole. Alternatively, both the macrophage and phagosomal vesicles contained within are disrupted and the released bacteria are analysed by FACS.

[0036] Suitable macrophage cells include human acute-monocytic leukemic cell lines of macrophage lineage: CD14⁺, CD15⁺ (THP-1), murine bone marrow-derived macrophage cell lines, and murine BALB/c tumour derived macrophage-monocyte cell lines (eg. ATCC TIB-67, and ATCC TIB-71).

[0037] Example 3 of the present application describes one preferred macrophage assay of the present application. However, any one of numerous conventional macrophage infection assays may be employed in the present invention.

[0038] Suitable media for culturing mycobacteria under non-virulence conditions are described in Wayne, L. G. (1994) [in Tuberculosis: Pathogenesis, Protection, and Control published by the American Society for Microbiology, pp. 73-83]. These include Middlebrook 7H9 Medium [see Barker, L. P., et al. (1998) Molec. Microbiol., vol. 29(5), pp. 1167-1177, and WO00/52139 in the name of the present Applicant].

[0039] In use, an induced or up-regulated promoter is identified by detecting increased expression of the reporter sequence during macrophage infection when compared to expression of the reporter sequence under culture conditions which do not promote mycobacterial virulence. This minimises the risk of identifying mycobacterial host cells containing putative promoters which are constitutively expressed.

[0040] Suitable culture conditions which do not promote mycobacterial virulence (ie. conditions which support non-virulence) include mycobacterial culture conditions which are substantially free from macrophage.

[0041] In one embodiment, the non-virulence culture conditions are substantially non-limiting in terms of aerobic growth (eg. pH, temperature, and available nutrients) of the mycobacterial host cell culture. Thus, the mycobacterial host cell culture is preferably cultured under conventional conditions which permit a doubling time of 18-26 hours.

[0042] In use, the mycobacterial host cell culture may be cultured in batch, and is preferably harvested during mid- to late-exponential phase. Alternatively, this point in the growth phase may be mimicked under continuous culture conditions employing a steady state growth rate approximating μ_(max) which provides a generation time of approximately 18-24 hours.

[0043] The preferred culture method employed by the present invention is that of batch fermenter culture. This method permits careful monitoring of growth culture parameters such as pH, temperature, available nutrients, and dissolved oxygen tension (DOT). In particular, temperature and DOT may be strictly controlled.

[0044] The identification of transformed host cells containing promoters which are constitutively expressed may be performed before or after identification of promoters expressed during virulence conditions. In a preferred embodiment, constitutively expressed promoters are identified after identification of induced or up-regulated promoters expressed during virulence.

[0045] Increased expression means that the signal detected as a result of expression of the reporter sequence when the mycobacterial host cell is cultured under virulence conditions is at least 1.3 times greater than the signal detected when the host cell is cultured under non-virulence conditions. In one embodiment, the signal is at least 2 times, preferably at least 4 times greater when the host cell is cultured under virulence conditions. In another embodiment, the signal is at least 10, preferably at least 20, and particularly preferably at least 30 times greater when the host cell is cultured under virulence conditions.

[0046] Naturally, the expression profile for a given gene in a mycobacterial host cell may vary during the course of infection. For example, a gene may be induced or up-regulated most strongly during the early stages of an infection. Thus, the term “increased expression” refers to the maximum signal obtained for a given reporter gene under virulence conditions vis-a-vis non-virulence conditions.

[0047] In one embodiment, the “increased expression” concerns the maximum signal obtained within the first four days after macrophage infection, preferably within the first two days after macrophage infection.

[0048] In another embodiment, genes switched on or up-regulated at later stages of infection are of interest, in which case a maximum signal 4 days after macrophage infection is preferred. For example, a maximum signal up to 11-12 days after infection may be preferred. However, due to the invasive and destructive nature of a M. tuberculosis infection on a macrophage, a post-infection period of between 4 and 6 days is particularly preferred.

[0049] A number of methods may be employed for obtaining putative mycobacterial promoter sequences for use in the present invention. These include:- generation of a library of putative promoter sequences by use of nucleic acid digestion enzymes (see Example 1); and identifying nucleic acid sequence homology to known virulence or previously implicated virulence sequences in other microorganisms (see Example 2).

[0050] In application of the above homology identification method, a single promoter construct (rather than a selection of constructs generated from a library) is prepared, and a promoter-reporter unit constructed. It is then possible to assess promoter activity by direct comparison (eg. by FACS) of mycobacterial host cultured under virulence conditions versus non-virulence conditions. Since only a single promoter-reporter construct is employed, there is no need for a separate screening of the host cells.

[0051] The method of the present invention permits identification of promoters which are induced or up-regulated during virulence. Once the nucleic acid sequence and orientation of a desirable promoter sequence has been determined, the exact location can be mapped by use of convention nucleic acid homology search computer software (eg. BLASTN, or BLASTX) performed on published sequences of the mycobacterial species concerned. Accordingly, the gene or operon under the control of the identified promoter may be identified.

[0052] Thus, in a second aspect of the present invention, there is provided a method of identifying a mycobacterial gene the expression of which is induced or up-regulated during mycobacterial virulence, said method comprising:

[0053] identifying a mycobacterial promoter sequence which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell, wherein the host cell contains a nucleic acid construct comprising said promoter sequence operably linked to a coding sequence of a reporter gene located down-stream from the promoter;

[0054] aligning by sequence homology the nucleic acid sequence of the promoter with published nucleic acid sequence data for the same mycobacterial species; and

[0055] identifying the associated nucleic acid coding sequence under the control of said promoter.

[0056] Reference to “gene” throughout this specification embraces open reading frames (ORFs).

[0057] According to a third aspect of the present invention there is provided an isolated mycobacterial peptide or a fragment or derivative or variant thereof, wherein the peptide is encoded by a mycobacterial gene the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said mycobacterial gene.

[0058] The various embodiments described for the first and second aspect of the present invention apply equally for the third and subsequent aspects of the present invention.

[0059] The terms “isolated,” “substantially pure,” and “substantially homogenous” are used interchangeably to describe a peptide which has been separated from components which naturally accompany it. A peptide is substantially pure when at least about 60 to 75% of a sample exhibits a single peptide sequence. A substantially pure peptide will typically comprise about 60 to 90% w/w of a protein sample, more usually about 95%, and preferably will be over about 99% pure. Peptide purity or homogeneity may be indicated by, for example, polyacrylamide gel electrophoresis of a protein sample, followed by visualizing a single polypeptide band upon staining the gel. Alternatively, higher resolution may be provided by using, for example, HPLC.

[0060] A peptide is considered to be isolated when it is separated from the contaminants which accompany it in its natural state. Thus, a peptide which is chemically synthesized or synthesized in a cellular system different from the cell from which it naturally originates will be substantially free from its naturally associated components.

[0061] The present invention provides peptides which may be purified from mycobacteria as well as from other types of cells transformed with recombinant nucleic acids encoding these peptides.

[0062] If desirable, the amino acid sequence of the proteins of the present invention may be determined by protein sequencing methods.

[0063] The terms “peptide”, “oligopeptide”, “polypeptide”, and “protein” are used interchangeably and do not refer to a specific length of the product. These terms embrace post-translational modifications such as glycosylation, acetylation, and phosphorylation.

[0064] The term “fragment” means a peptide having at least five, preferably at least ten, more preferably at least twenty, and most preferably at least thirty-five amino acid residues of the peptide which is the gene product of the induced or up-regulated gene in question. The fragment preferably includes at least one epitope of the gene product in question.

[0065] The term “variant” means a peptide or peptide “fragment” having at least seventy, preferably at least eighty, more preferably at least ninety percent amino acid sequence homology with the peptide which is the gene product of the induced or up-regulated peptide in question. An example of a “variant” is a peptide or peptide fragment of an induced/up-regulated gene which contains one or more analogs of an amino acid (eg. an unnatural amino acid), or a substituted linkage. The terms “homology” and “identity are considered synonymous in this specification. In a further embodiment, a “variant” may be a mimic of the peptide or peptide fragment, which mimic reproduces at least one epitope of the peptide or peptide fragment. The mimic may be, for example, a nucleic acid mimic, preferably a DNA mimic.

[0066] For sequence comparison, typically one sequence acts as a reference sequence, to which test sequences may be then compared. When using a sequence comparison algorithm, test and reference sequences are input into a computer, subsequent coordinates are designated, if necessary, and sequence algorithm program parameters are designated. The sequence comparison algorithm then calculates the percentage sequence identity for the test sequence(s) relative to the reference sequence, based on the designated program parameters.

[0067] Optimal alignment of sequences for comparison may be conducted, for example, by the local homology alignment algorithm of Smith and Waterman [Adv. Appl. Math. 2: 484 (1981)], by the algorithm of Needleman & Wunsch [J. Mol. Biol. 48: 443 (1970)] by the search for similarity method of Pearson & Lipman [Proc. Nat'l. Acad. Sci. USA 85: 2444 (1988)], by computer implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA—Sequence Analysis Software Package of the Genetics Computer Group, University of Wisconsin Biotechnology Center, 1710 University Avenue, Madison, Wis. 53705), or by visual inspection [see Current Protocols in Molecular Biology, F. M. Ausbel et al, eds, Current Protocols, a joint venture between Greene Publishing Associates, In. And John Wiley & Sons, Inc. (1995 Supplement) Ausbubel].

[0068] Examples of algorithms suitable for determining percent sequence similarity are the BLAST and BLAST 2.0 algorithms [see Altschul (1990) J. Mol. Biol. 215: pp. 403-410; and “http://www.ncbi.nim.nih.gov/” of the National Center for Biotechnology Information].

[0069] In a preferred homology comparison, the identity exists over a region of the sequences that is at least 10 amino acids, preferably at least 20 amino acids, more preferably at least 35 amino acids in length.

[0070] The term “derivative” means a protein comprising the peptide (or fragment, or variant thereof) which peptide is the gene product of the induced or up-regulated gene in question. Thus, a derivative may include the peptide in question, and a further peptide sequence which may introduce one or more additional epitopes. The further peptide sequence should preferably not interfere with the basic folding and thus conformational structure of the peptide in question. Examples of a “derivative” are a fusion protein, a conjugate, and a graft. Thus, two or more peptides (or fragments, or variants) may be joined together to form a derivative. Alternatively, a peptide (or fragment, or variant) may be joined to an unrelated molecule (eg. a second, unrelated peptide). Derivatives may be chemically synthesized, but will be typically prepared by recombinant nucleic acid methods. Additional components such as lipid, and/or polysaccharide, and/or polyketide components may be included.

[0071] All of the molecules “fragment”, “variant” and “derivative” have a common antigenic cross-reactivity and/or substantially the same in vivo biological activity as the peptide product of the induced or up-regulated gene in question from which they are derived. For example, an antibody capable of binding to a fragment, variant or derivative would be also capable of binding to the gene product of the induced or up-regulated gene in question. It is a preferred feature that the fragment, variant and derivative each possess the active site of the peptide which is the induced or up-regulated peptide in question. Alternatively, all of the above embodiments of a peptide of the present invention share a common ability to induce a “recall response” of a T-lymphocyte which has been previously exposed to an antigenic component of a mycobacterial infection.

[0072] In a preferred embodiment, the peptide is selected from the group consisting of SEQ ID NO: 2; 4; 6; 8; 10; 12; 14; 16; 19; 21; 23; 25; 27; 29; 31; 33; 35; 38; 40; 42; 44; 46; 48;-50; 52; 55; 58; 60; 62; 64; 67; 69; 72; 75; 78; 80; 82; 85; 87; 89; 92; 94; 97; 100; 103; 105; 107; 109; 111; 113; 115; and 117.

[0073] A fourth aspect of the invention provides an inhibitor of a mycobacterial peptide, wherein the peptide is encoded by a mycobacterial gene the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said mycobacterial gene, and wherein the inhibitor is capable of substantially preventing or inhibiting the mycobacterial peptide from exerting its native biological function or effect.

[0074] Inhibition of the mycobacterial peptide may be effected at the nucleic acid level (ie. DNA, or RNA), or at the peptide level.

[0075] In a further embodiment, the inhibitor may be an antibiotic capable of targeting the induced or up-regulated mycobacterial gene, or the peptide product thereof. The antibiotic is preferably specific for the gene and/or peptide product.

[0076] Inhibitors of the present invention may be prepared utilizing the sequence information provided herein. For example, this may be performed by overexpressing the peptide, purifying the peptide, and then performing X-ray compounds are created which have similar molecular structures to all or portions of the peptide or its substrate. The compounds may be then combined with the peptide and attached thereto so as to block one or more of its biological activities.

[0077] Also included within the invention are isolated or recombinant polynucleotides that bind to the regions of the mycobacterial chromosome (eg. promoter, or coding region), or transcription products thereof, containing sequences that are associated with induction/up-regulation of a mycobacterial gene during macrophage infection by M. tuberculosis, including antisense and triplex forming polynucleotides. As used herein, the term “binding” refers to an interaction or complexation between an oligonucleotide and a target nucleotide sequence, mediated through hydrogen bonding or other molecular forces. The term “binding” more specifically refers to two types of internucleotide binding mediated through base-base hydrogen bonding. The first type of binding is “Watson-Crick-type” binding interactions in which adenine-thymine (or adenine-uracil) and guanine-cytosine base-pairs are formed through hydrogen bonding between the bases. An example of this type of binding is the binding traditionally associated with the DNA double helix and in RNA-DNA hybrids; this type of binding is normally detected by hybridization procedures.

[0078] A second type of binding is “triplex binding”. In general, triplex binding refers to any type of base-base hydrogen bonding of a third polynucleotide strand with a duplex DNA (or DNA-RNA hybrid) that is already paired in a Watson-Crick manner.

[0079] In a preferred embodiment, the inhibitor may be an antisense nucleic acid sequence which is complementary to at least part of the inducible or up-regulatable gene.

[0080] The inhibitor, when in the form of a nucleic acid sequence, comprises, in use, at least 15 nucleotides, preferably at least 20 nucleotides, more preferably at least 30 nucleotides, and most preferably at least 50 nucleotides.

[0081] In a fifth aspect there is provided an antibody which binds to a peptide encoded by a gene, or to a fragment or variant or derivative of said peptide, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene,

[0082] The antibody preferably has specificity for the peptide in question, and following binding thereto may initiate coating of a mycobacterium expressing said peptide. Coating of the bacterium preferably leads to opsonization thereof. This, in turn, leads to the bacterium being destroyed. It is preferred that the antibody is specific for the mycobacterium (eg. species and/or strain) which is to be targeted.

[0083] Opsonization by antibodies may influence cellular entry and spread of mycobacteria in phagocytic and non-phagocytic cells by preventing or modulating receptor-mediated entry and replication in macrophages.

[0084] The peptides, fragments, variants or derivatives of the present invention may be used to produce antibodies, including polyclonal and monoclonal. If polyclonal antibodies are desired, a selected mammal (eg. mouse, rabbit, goat, horse, etc.) is immunized with an immunogenic polypeptide. Serum from the immunized animal is collected and treated according to known procedures. If serum containing polyclonal antibodies to a desired mycobacterial epitope contains antibodies to other antigens, the polyclonal antibodies may be purified by immunoaffinity chromatography.

[0085] Alternatively, general methodology for making monoclonal antibodies by hybridomas involving, for example, preparation of immortal antibody-producing cell lines by cell fusion, or other techniques such as direct transformation of B lymphocytes with oncogenic DNA, or transfection with Epstein-Barr virus may be employed.

[0086] The antibody employed in this aspect of the invention may belong to any antibody isotype family, or may be a derivative or mimic thereof. Reference to antibody throughout this specification embraces recombinantly produced antibody, and any part of an antibody which is capable of binding to a mycobacterial antigen.

[0087] In one embodiment the antibody belongs to the IgG, IgM or IgA isotype families.

[0088] In a preferred embodiment, the antibody belongs to the IgA isotype family. Reference to the IgA isotype throughout this specification includes the secretory form of this antibody (ie. sigA). The secretory component (SC) of sigA may be added in vitro or in vivo. In the latter case, the use of a patient's natural SC labelling machinery may be employed.

[0089] In one embodiment, the antibody may be raised against a peptide from a member of the MTC, preferably against M. tuberculosis.

[0090] In a preferred embodiment, the antibody is capable of binding to a peptide selected from the group consisting of SEQ ID NO: 2; 4; 6; 8; 10; 12; 14; 16; 19; 21; 23; 25; 27; 29; 31; 33; 35; 38; 40; 42; 44; 46; 48; 50; 52; 55; 58; 60; 62; 64; 67; 69; 72; 75; 78; 80; 82; 85; 87; 89; 92; 94; 97; 100; 103; 105; 107; 109; 111; 113; 115; and 117 (or fragment, variant, of derivative thereof). The antibodies of the present invention are preferably employed in an isolated form.

[0091] In a further embodiment, the antigen is an exposed component of a mycobacterial bacillus. In another embodiment, the antigen is a cell surface component of a mycobacterial bacillus.

[0092] The antibody of the present invention may be polyclonal, but is preferably monoclonal.

[0093] Without being bound by any theory, it is possible that following mycobacterial infection of a macrophage, the macrophage is killed and the bacilli are released. It is at this stage that the mycobacteria are considered to be most vulnerable to antibody attack. Thus, it is possible that the antibodies of the present invention act on released bacilli following macrophage death, and thereby exert a post-infection effect.

[0094] It is possible that the passive protection aspect (ie. delivery of antibodies) of the present invention is facilitated by enhanced accessibility of the antibodies of the present invention to antigens on mycobacterial bacilli. It is possible that antibody binding may block macrophage infection by steric hindrance or disruption of its oligomeric structure. Thus, antibodies acting on mycobacterial bacilli released from killed, infected macrophages may interfere with the spread of re-infection to fresh macrophages. This hypothesis involves a synergistic action between antibodies and cytotoxic T cells, acting early after infection, eg. γ{overscore (o)} and NK T cells, but could later involve also CD8 and CD4 cytotoxic T cells.

[0095] According to a sixth aspect of the invention there is provided an attenuated mycobacterium in which a gene has been modified, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said mycobacterial gene, thereby rendering the mycobacterium substantially non-pathogenic.

[0096] The term “modified” refers to any genetic manipulation such as a nucleic acid or nucleic acid sequence replacement, a deletion, or an insertion which renders the mycobacterium substantially non-pathogenic or substantially incapable of macrophage infection. In one embodiment the entire inducible or up-regulatable gene may be deleted.

[0097] In one embodiment, the modification may be effected by a nucleic acid sequence encoding an anti-sense nucleic acid sequence to the induced or up-regulated gene, or a transcription product thereof. Thus, by including such a nucleic acid sequence in a mycobacterium, for example in the form of a plasmid, expression of the peptide product of the induced or up-regulated gene may be reduced or substantially inhibited.

[0098] In a preferred embodiment, the gene to be modified has a wild-type coding sequence corresponding to one of the group consisting of SEQ ID NO: 3; 5; 7; 9; 11; 13; 15; 17; 20; 22; 24; 26; 28; 30; 32; 34; 36; 39; 41; 43; 45; 47; 49; 51; 53; 56; 59; 61; 63; 65; 68; 70; 73; 76; 79; 81; 83; 86; 88; 90; 93; 95; 98; 101; 104; 106; 108; 110; 112; 114; 116; and 118.

[0099] It will be appreciated that the wild-type sequences may include minor variations depending on the Database employed. Reference to wild-type simply means that the sequence in question occurs in nature.

[0100] A seventh aspect of the present invention provides an attenuated microbial carrier, comprising a peptide encoded by a gene, or a fragment or variant or derivative of said peptide, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene.

[0101] In use, the peptide (or fragment, variant or derivative) is either at least partially exposed at the surface of the carrier, or the carrier becomes degraded in vivo so that at least part of the peptide (or fragment, variant or derivative) is otherwise exposed to a host's immune system.

[0102] In a preferred embodiment, the peptide is selected from the group consisting of SEQ ID NO: 2; 4; 6; 8; 10; 12; 14; 16; 19; 21; 23; 25; 27; 29; 31; 33; 35; 38; 40; 42; 44; 46; 48; 50; 52; 55; 58; 60; 62; 64; 67; 69; 72; 75; 78; 80; 82; 85; 87; 89; 92; 94; 97; 100; 103; 105; 107; 109; 111; 113; 115; and 117.

[0103] In one embodiment, the attenuated microbial carrier is selected from the group consisting of attenuated salmonella, attenuated vaccinia virus, attenuated fowlpox virus, or attenuated M. bovis (eg. BCG strain).

[0104] According to an eighth aspect of the invention there is provided a DNA plasmid comprising a promoter, a polyadenylation signal, and a DNA sequence which corresponds to the coding sequence of a mycobacterial gene, or a fragment or variant or derivative of said DNA sequence, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said mycobacterial gene, wherein the promoter and polyadenylation signal are operably linked to the DNA sequence.

[0105] The term DNA fragment” used in this invention will usually comprise at least about 5 codons (15 nucleotides), more usually at least about 7 to 15 codons, and preferably at least about 35 codons. This number of nucleotides is usually about the minimal length required for a successful probe that would hybridize specifically with such a sequence.

[0106] In preferred embodiments, the DNA “fragment” has a nucleotide length which is at least 50%, preferably at least 70%, and more preferably at least 80% that of the coding sequence of the corresponding induced/up-regulated gene.

[0107] The term DNA “variant” means a DNA sequence which has substantial homology or substantial similarity to the coding sequence (or a fragment “substantially homologous” (or “substantially similar”) to another if, when optimally aligned (with appropriate nucleotide insertions or deletions) with the other nucleic acid (or its complementary strand), there is nucleotide sequence identity in at least about 60% of the nucleotide bases, usually at least about 70%, more usually at least about 80%, preferably at least about 90%, and more preferably at least about 95 to 98% of the nucleotide bases. Homology determination is performed as described supra for peptides.

[0108] Alternatively, a DNA “variant” is substantially homologous (or substantially similar) with the coding sequence (or a fragment thereof) of an induced/up-regulated gene when they are capable of hybridizing under selective hybridization conditions. Selectivity of hybridization exists when hybridization occurs which is substantially more selective than total lack of specificity. Typically, selective hybridization will occur when there is at least about 65% homology over a stretch of at least about 14 nucleotides, preferably at least about 70%, more preferably at least about 75%, and most preferably at least about 90%. See, Kanehisa (1984) Nuc. Acids Res. 12:203-213. The length of homology comparison, as described, may be over longer stretches, and in certain embodiments will often be over a stretch of at least about 17 nucleotides, usually at least about 20 nucleotides, more usually at least about 24 nucleotides, typically at least about 28 nucleotides, more typically at least about 32 nucleotides, and preferably at least about 36 or more nucleotides.

[0109] Nucleic acid hybridization will be affected by such conditions as salt concentration (eg. NaCl), temperature, or organic solvents, in addition to the base composition, length of the complementary strands, and the number of nucleotide base mismatches between the hybridizing nucleic acids, as will be readily appreciated by those skilled in the art. Stringent temperature conditions are preferably employed, and generally include temperatures in excess of 30° C., typically in excess of 37° C. and preferably in excess of 45° C. Stringent salt conditions will ordinarily be less than 1000 mM, typically less than 500 mM, and preferably less than 200 mM. The pH is typically between 7.0 and 8.3. However, the combination of parameters is much more important than the measure of any single parameter. See, eg., Wetmur and Davidson (1968) J. Mol. Biol. 31:349-370.

[0110] The term DNA “derivative” means a DNA polynucleotide which comprises a DNA sequence (or a fragment, or variant thereof) corresponding to the coding sequence of the induced/up-regulated gene and an additional DNA sequence which is not naturally associated with the DNA sequence corresponding to the coding sequence. The comments on peptide derivative supra also apply to DNA “derivative”. A “derivative” may, for example, include two or more coding sequences of a mycobacterial operon which is induced during macrophage infection. Thus, depending on the presence or absence of a non-coding region between the coding sequences, the expression product/s of such a “derivative” may be a fusion protein, or separate peptide products encoded by the individual coding regions.

[0111] The above terms DNA “fragment”, “variant”, and “derivative” have in common with each other that the resulting peptide products have cross-reactive antigenic properties which are substantially the same as those of the corresponding wild-type peptide. Preferably all of the peptide products of the above DNA molecule embodiments of the present invention bind to an antibody which also binds to the wild-type peptide. Alternatively, all of the above peptide products are capable of inducing a “recall response” of a T lymphocyte which has been previously exposed to an antigenic component of a mycobacterial infection.

[0112] The promoter and polyadenylation signal are preferably selected so as to ensure that the gene is expressed in a eukaryotic cell. Strong promoters and polyadenylation signals are preferred.

[0113] In a related aspect, the present invention provides an isolated RNA molecule which is encoded by a DNA sequence of the present invention, or a fragment or variant or derivative of said DNA sequence.

[0114] An “isolated” RNA is an RNA which is substantially separated from other mycobacterial components that naturally accompany the sequences of interest, eg., ribosomes, polymerases, and other mycobacterial polynucleotides such as DNA and other chromosomal sequences.

[0115] The above RNA molecule may be introduced directly into a host cell as, for example, a component of a vaccine.

[0116] Alternatively the RNA molecule may be incorporated into an RNA vector prior to administration.

[0117] The polynucleotide sequences (DNA and RNA) of the present invention include a nucleic acid sequence which has been removed from its naturally occurring environment, and recombinant or cloned DNA isolates and chemically synthesized analogues or analogues biologically synthesized by heterologous systems.

[0118] The term “recombinant” as used herein intends a polynucleotide of genomic, cDNA, semisynthetic, or synthetic origin which, by virtue of its origin or manipulation: (1) is not associated with all or a portion of a polynucleotide with which it is associated in nature; or (2) is linked to a polynucleotide other than that to which it is linked in nature; and (3) does not occur in nature. This artificial combination is often accomplished by either chemical synthesis means, or by the artificial manipulation of isolated segments of nucleic acids, eg., by genetic engineering techniques. Such is usually done to replace a codon with a redundant codon encoding the same or a conservative amino acid, while typically introducing or removing a sequence recognition site. Alternatively, it is performed to join together nucleic acid segments of desired functions to generate a desired combination of functions.

[0119] In embodiments of the invention the polynucleotides may encode a peptide which is induced or up-regulated during macrophage infection. A nucleic acid is said to “encode” a peptide if, in its native state or when manipulated, it can be transcribed and/or translated to produce the peptide or a fragment or variant or derivative thereof. The anti-sense strand of such a nucleic acid is also said to encode the sequence.

[0120] Also contemplated within the invention are expression vectors comprising the polynucleotide of interest. Expression vectors generally are replicable polynucleotide constructs that encode a peptide operably linked to suitable transcriptional and translational regulatory elements. Examples of regulatory elements usually included in expression vectors are promoters, enhancers, ribosomal binding sites, and transcription and translation initiation and termination sequences. These regulatory elements are operably linked to the sequence to be translated. A nucleic acid sequence is operably linked when it is placed into a functional relationship with another nucleic acid sequence. For instance, a promoter is operably linked to a coding sequence if the promoter affects its transcription or expression. Generally, operably linked means that the DNA sequences being linked are contiguous and, where necessary to join two protein coding regions, contiguous and in reading frame. The regulatory elements employed in the expression vectors containing a polynucleotide encoding a virulence factor are functional in the host cell used for expression.

[0121] The polynucleotides of the present invention may be prepared by any means known in the art. For example, large amounts of the polynucleotides may be produced by replication in a suitable host cell. The natural or synthetic DNA fragments coding for a desired fragment will be incorporated into recombinant nucleic acid constructs, typically DNA constructs, capable of introduction into and replication in a prokaryotic or eukaryotic cell. Usually the DNA constructs will be suitable for autonomous replication in a unicellular host, such as yeast or bacteria, but may also be intended for introduction to and integration within the genome of a cultured insect, mammalian, plant or other eukaryotic cell lines.

[0122] The polynucleotides of the present invention may also be produced by chemical synthesis, eg. by the phosphoramidite method or the triester method, and may be performed on commercial automated oligonucleotide synthesizers. A double-stranded fragment may be obtained from the single stranded product of chemical synthesis either by synthesizing the complementary strand and annealing the strand together under appropriate conditions or by adding the complementary strand using DNA polymerase with an appropriate primer sequence.

[0123] DNA constructs prepared for introduction into a prokaryotic or eukaryotic host will typically comprise a replication system recognized by the host, including the intended DNA fragment encoding the desired peptide, and will preferably also include transcription and translational initiation regulatory sequences operably linked to the polypeptide encoding segment. Expression vectors may include, for example, an origin of replication or autonomously replicating sequence (ARS) and expression control sequences, a promoter, an enhancer and necessary processing information sites, such as ribosome-binding sites, RNA splice sites, polyadenylation sites, transcriptional terminator sequences, and mRNA stabilizing sequences. Secretion signals from polypeptides secreted from the host cell of choice may also be included where appropriate, thus allowing the protein to cross and/or lodge in cell membranes, and thus attain its functional topology or be secreted from the cell.

[0124] An appropriate promoter and other necessary vector sequences will be selected so as to be functional in the host, and may, when appropriate, include those naturally associated with mycobacterial genes. Promoters such as the trp, lac and phage promoters, tRNA promoters and glycolytic enzyme promoters may be used in prokaryotic hosts. Useful yeast promoters include the promoter regions for metallothionein, 3-phosphoglycerate kinase or other glycolytic enzymes such as enolase or glyceraldehyde-3-phosphate dehydrogenase, enzymes responsible for maltose and galactose utilization, and others.

[0125] Appropriate non-native mammalian promoters might include the early and late promoters from SV40 or promoters derived from human cytomegalovirus, murine moloney leukemia virus, mouse mammary tumour virus, avian sarcoma viruses, adenovirus II, bovine papilloma virus or polyoma. In addition, the construct may be joined to an amplifiable gene (e.g., DHFR) so that multiple copies of the gene may be made.

[0126] While such expression vectors may replicate autonomously, they may less preferably replicate by being inserted into the genome of the host cell.

[0127] Expression and cloning vectors will likely contain a selectable marker, a gene encoding a protein necessary for the survival or growth of a host cell transformed with the vector. The presence of this gene ensures the growth of only those host cells which express the inserts. Typical selection genes encode proteins that (a) confer resistance to antibiotics or other toxic substances, e.g. ampicillin, kanamycin, neomycin, methotrexate, etc.; (b) complement auxotrophic deficiencies; or (c) supply critical nutrients not available from complex media, e.g. the gene encoding D-alanine racemase for Bacilli. The choice of appropriate selectable marker will depend on the host cell.

[0128] The vectors containing the nucleic acids of interest can be transcribed in vitro and the resulting RNA introduced into the host cell (e.g., by injection), or the vectors can be introduced directly into host cells by methods which vary depending on the type of cellular host, including electroporation; transfection employing calcium chloride, rubidium chloride calcium phosphate, DEAE-dextran, or other substances; microprojectile bombardment; lipofection; infection (where the vector is an infectious agent, such as a retroviral genome). The cells into which have been introduced nucleic acids described above are meant to also include the progeny of such cells.

[0129] Large quantities of the nucleic acids and peptides of the present invention may be prepared by expressing the nucleic acids or portions thereof in vectors or other expression vehicles in compatible prokaryotic or eukaryotic host cells. The most commonly used prokaryotic hosts are strains of Escherichia coli, although other prokaryotes, such as Bacillus subtilis or Pseudomonas may also be used.

[0130] Mammalian or other eukaryotic host cells, such as those of yeast, filamentous fungi, plant, insect, amphibian or avian species, may also be useful for production of the proteins of the present invention. Propagation of mammalian cells in culture is per se well known. Examples of commonly used mammalian host cell lines are VERO and HeLa cells, Chinese hamster ovary (CHO) cells, and WI38, BHK, and COS cell lines, although other cell lines may be appropriate, e.g., to provide higher expression, desirable glycosylation patterns.

[0131] Clones are selected by using markers depending on the mode of the vector construction. The marker may be on the same or a different DNA molecule, preferably the same DNA molecule. The transformant may be screened or, preferably, selected by any of the means well known in the art, e.g., by resistance to such antibiotics as ampicillin, tetracycline.

[0132] The polynucleotides of the invention may be inserted into the host cell by any means known in the art, including for example, transformation, transduction, and electroporation. As used herein, “recombinant host cells”, “host cells”, “cells”, “cell lines”, “cell cultures”, and other such terms denoting microorganisms or higher eukaryotic cell lines cultured as unicellular entities refer to cells which can be, or have been, used as recipients for recombinant vector or other transfer DNA, and include the progeny of the original cell which has been transformed. It is understood that the progeny of a single parental cell may not necessarily be completely identical in morphology or in genomic or total DNA complement as the original parent, due to natural, accidental, or deliberate mutation. “Transformation”, as used herein, refers to the insertion of an exogenous polynucleotide into a host cell, irrespective of the method used for the insertion, for example, direct uptake, transduction, f-mating or electroporation. The exogenous polynucleotide may be maintained as a non-integrated vector, for example, a plasmid, or alternatively, may be integrated into the host cell genome.

[0133] In one embodiment, a DNA plasmid or RNA vector may encode a component of the immune system which is specific to an immune response following challenge with a peptide, wherein said peptide is encoded by a mycobacterial gene which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said mycobacterial gene.

[0134] An example of such a component is an antibody to the peptide product of an induced or up-regulated gene. Thus, in this embodiment, the nucleic acid sequence (eg. DNA plasmid or RNA vector) encodes the antibody in question.

[0135] A ninth aspect provides use of a peptide, an inhibitor, an antibody, an attenuated mycobacterium, an attenuated microbial carrier, a DNA sequence corresponding to the coding sequence of an induced or up-regulated gene or a fragment or variant or derivative of said DNA sequence, a DNA plasmid comprising said DNA sequence or said fragment or variant or derivative, an RNA sequence encoded by said DNA sequence or said fragment or variant or derivative, and/or an RNA vector comprising said RNA sequence, according to the present invention, in the manufacture of a medicament for treating or preventing a mycobacterial infection.

[0136] The term “treating” includes post-infection therapy and amelioration of a mycobacterial infection.

[0137] The term “preventing” includes reducing the severity/intensity of, or initiation of, a mycobacterial infection.

[0138] In a related aspect, there is provided a method of treating or preventing a mycobacterial infection, comprising administration of a medicament selected from the group consisting of a peptide, an inhibitor, an antibody, an attenuated mycobacterium, an attenuated microbial carrier, a DNA sequence corresponding to the coding sequence of an induced or up-regulated gene or a fragment or variant or derivative of said DNA sequence, a DNA plasmid comprising said DNA sequence or said fragment or variant or derivative, an RNA sequence encoded by said DNA sequence or said fragment or variant or derivative, and/or an RNA vector comprising said RNA sequence, according to the present invention, to a patient.

[0139] The medicament may be administered by conventional routes, eg. intravenous, intraperitoneal, intranasal routes.

[0140] The immunogenicity of the epitopes of the peptides of the invention may be enhanced by preparing them in mammalian or yeast systems fused with or assembled with particle-forming proteins such as, for example, that associated with hepatitis B surface antigen. Vaccines may be prepared from one or more immunogenic peptides of the present invention.

[0141] Typically, such vaccines are prepared as injectables, either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid prior to injection may also be prepared. The preparation may also be emulsified, or the peptide encapsulated in liposomes. The active immunogenic ingredients are often mixed with excipients which are pharmaceutically acceptable and compatible with the active ingredient. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like and combinations thereof. In addition, if desired, the vaccine may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents, and/or adjuvants which enhance the effectiveness of the vaccine. Examples of adjuvants which may be effective include but are not limited to: aluminum hydroxide, N-acetyl-muramyl-L-threonyl-D-isoglutamine (thr-MDP), N-acetyl-nor-muramyl-L-alanyl-D-isoglutamine (CGP 11637, referred to as nor-MDP), N-acetylmuramyl-L-alanyl-D-isoglutaminyl-L-alanine-2-(7′-1′-2′-dipalm itoyl-sn-glycero-3-hydroxyphosphoryloxy)-ethylamine (CGP 19835A, referred to as MTP-PE), and RIBI, which contains three components extracted from bacteria, monophosphoryl lipid A, trehalose dimycolate and cell wall skeleton (MPL+TDM+CWS) in a 2% squalene/Tween 80 emulsion.

[0142] The vaccines are conventionally administered parenterally, by injection, for example, either subcutaneously or intramuscularly. Additional formulations which are suitable for other modes of administration include suppositories and, in some cases, oral formulations or formulations suitable for distribution as aerosols. For suppositories, traditional binders and carriers may include, for example, polyalkylene glycols or triglycerides; such suppositories may be formed from mixtures containing the active ingredient in the range of 0.5% to 10%, preferably 1%-2%. Oral formulations include such normally employed excipients as, for example, pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, and the like. These compositions take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations or powders and contain 10% -95% of active ingredient, preferably 25%-70%.

[0143] The peptides may be formulated into the vaccine as neutral or salt forms. Pharmaceutically acceptable salts include the acid addition salts (formed with free amino groups of the peptide) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or with organic acids such as acetic, oxalic, tartaric, maleic, and the like. Salts formed with the free carboxyl groups may also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like.

[0144] The vaccines are administered in a manner compatible with the dosage formulation, and in such amount as will be prophylactically and/or therapeutically effective. The quantity to be administered, which is generally in the range of 5 micrograms to 250 micrograms of antigen per dose, depends on the subject to be treated, capacity of the subject's immune system to synthesize antibodies, and the degree of protection desired. Precise amounts of active ingredient required to be administered may depend on the judgment of the practitioner and may be peculiar to each subject.

[0145] The vaccine may be given in a single dose schedule, or preferably in a multiple dose schedule. A multiple dose schedule is one in which a primary course of vaccination may be with 1-10 separate doses, followed by other doses given, at subsequent time intervals required to maintain and or reenforce the immune response, for example, at 1-4 months for a second dose, and if needed, a subsequent dose(s) after several months. The dosage regimen will also, at least in part, be determined by the need of the individual and be dependent upon the judgment of the practitioner.

[0146] In addition, the vaccine containing the immunogenic mycobacterial antigen(s) may be administered in conjunction with other immunoregulatory agents, for example, immune globulins or cytokines, as well as antibiotics.

[0147] The outcome of administering antibody-containing compositions may depend on the efficiency of transmission of antibodies to the site of infection. In the case of a mycobacterial respiratory infection (eg. a M. tuberculosis infection), this may be facilitated by efficient transmission of antibodies to the lungs.

[0148] In one embodiment the medicament may be administered intranasally (i.n.). This mode of delivery corresponds to the route of delivery of a M. tuberculosis infection and, in the case of antibody delivery, ensures that antibodies are present at the site of infection to combat the bacterium before it becomes intracellular and also during the period when it spreads between cells.

[0149] An intranasal composition may be administered in droplet form having approximate diameters in the range of 100-5000 μm, preferably 500-4000 μm, more preferably 1000-3000 μm. Alternatively, in terms of volume, the droplets would be in the approximate range of 0.001-100 μl, preferably 0.1-50 μl, more preferably 1.0-25 μl.

[0150] Intranasal administration may be achieved by way of applying nasal droplets or via a nasal spray.

[0151] In the case of nasal droplets, the droplets may typically have a diameter of approximately 1000-3000 μm and/or a volume of 1-25 μl.

[0152] In the case of a nasal spray, the droplets may typically have a diameter of approximately 100-1000 μm and/or a volume of 0.001-1 μl.

[0153] It is possible that, following i.n. delivery of antibodies, their passage to the lungs is facilitated by a reverse flow of mucosal secretions, although mucociliary action in the respiratory tract is thought to take particles within the mucus out of the lungs. The relatively long persistence in the lungs, fast clearance from the bile and lack of transport to the saliva of some antibodies suggest the role of mucosal site specific mechanisms.

[0154] In a different embodiment, the medicament may be delivered in an aerosol formulation. The aerosol formulation may take the form of a powder, suspension or solution.

[0155] The size of aerosol particles is one factor relevant to the delivery capability of an aerosol. Thus, smaller particles may travel further down the respiratory airway towards the alveoli than would larger particles. In one embodiment, the aerosol particles have a diameter distribution to facilitate delivery along the entire length of the bronchi, bronchioles, and alveoli. Alternatively, the particle size distribution may be selected to target a particular section of the respiratory airway, for example the alveoli.

[0156] The aerosol particles may be delivered by way of a nebulizer or nasal spray.

[0157] In the case of aerosol delivery of the medicament, the particles may have diameters in the approximate range of 0.1-50 μm, preferably 1-25 μm, more preferably 1-5 μm.

[0158] The aerosol formulation of the medicament of the present invention may optionally contain a propellant and/or surfactant.

[0159] By controlling the size of the droplets which are to be administered to a patient to within the defined range of the present invention, it is possible to avoid/minimise inadvertent antigen delivery to the alveoli and thus avoid alveoli-associated pathological problems such as inflammation and fibrotic scarring of the lungs.

[0160] I.n. vaccination engages both T and B cell mediated effector mechanisms in nasal and bronchus associated mucosal tissues, which differ from other mucosae-associated lymphoid tissues.

[0161] The protective mechanisms invoked by the intranasal route of administration may include: the activation of T lymphocytes with preferential lung homing; upregulation of co-stimulatory molecules, eg. B7.2; and/or activation of macrophages or secretory IgA antibodies.

[0162] Intranasal delivery of antigens may facilitate a mucosal antibody response which is favoured by a shift in the T cell response toward the Th2 phenotype which helps antibody production. A mucosal response is characterised by enhanced IgA production, and a Th2 response is characterised by enhanced IL-4 production.

[0163] Intranasal delivery of mycobacterial antigens allows targeting of the antigens to submucosal B cells of the respiratory system. These B cells are the major local IgA-producing cells in mammals and intranasal delivery facilitates a rapid increase in IgA production by these cells against the mycobacterial antigens.

[0164] In one embodiment administration of the medicament comprising a mycobacterial antigen stimulates IgA antibody production, and the IgA antibody binds to the mycobacterial antigen. In another embodiment, a mucosal and/or Th2 immune response is stimulated.

[0165] In another embodiment monoclonal antibodies, in particular, may be used to raise anti-idiotype antibodies. Anti-idiotype antibodies are immunoglobulins which carry an “internal image” of the antigen of the infectious agent against which protection is desired. These anti-idiotype antibodies may also be useful for treatment, vaccination and/or diagnosis of mycobacterial infections.

[0166] According to a tenth aspect, the peptides (including fragments, derivatives, and variants thereof) of the present invention and antibodies to them are useful in immunoassays to detect the presence of antibodies to mycobacteria or the presence of the virulence associated antigens in biological samples.

[0167] Design of the immunoassays is subject to a great deal of variation, and many formats are known in the art. The immunoassay may utilize at least one epitope derived from a peptide of the present invention. In one embodiment, the immunoassay uses a combination of such epitopes. These epitopes may be derived from the same or from different bacterial peptides, and may be in separate recombinant or natural peptides, or together in the same recombinant peptides.

[0168] An immunoassay may use, for example, a monoclonal antibody directed towards a virulence associated peptide epitope(s), a combination of monoclonal antibodies directed towards epitopes of one mycobacterial antigen, monoclonal antibodies directed towards epitopes of different mycobacterial antigens, polyclonal antibodies directed towards the same antigen, or polyclonal antibodies directed towards different antigens.

[0169] Protocols may be based, for example, upon competition, or direct reaction, or sandwich type assays. Protocols may also, for example, use solid supports, or may be by immunoprecipitation. Most assays involve the use of labelled antibody or polypeptide; the labels may be, for example, enzymatic, fluorescent, chemiluminescent, radioactive, or dye molecules. Assays which amplify the signals from the probe are also known; examples of which are assays which utilize biotin and avidin, and enzyme-labeled and mediated immunoassays, such as ELISA assays.

[0170] Typically, an immunoassay for an antibody(s) to a peptide, will involve selecting and preparing the test sample suspected of containing the antibodies, such as a biological sample, then incubating it with an antigenic (i.e., epitope-containing) peptide(s) under conditions that allow antigen-antibody complexes to form, and then detecting the formation of such complexes. The immunoassay may be of a standard or competitive type.

[0171] The peptide is typically bound to a solid support to facilitate separation of the sample from the peptide after incubation. Examples of solid supports that can be used are nitrocellulose (eg. in membrane or microtiter well form), polyvinyl chloride (eg. in sheets or microtiter wells), polystyrene latex (eg. in beads or microtiter plates, polyvinylidine fluoride (known as Immulon), diazotized paper, nylon membranes, activated beads, and Protein A beads. For example, Dynatech Immulon microtiter plates or 60 mm diameter polystyrene beads (Precision Plastic Ball) may be used. The solid support containing the antigenic peptide is typically washed after separating it from the test sample, and prior to detection of bound antibodies.

[0172] Complexes formed comprising antibody (or, in the case of competitive assays, the amount of competing antibody) are detected by any of a number of known techniques, depending on the format. For example, unlabeled antibodies in the complex may be detected using a conjugate of antixenogeneic Ig complexed with a label (eg. an enzyme label).

[0173] In immunoassays where the peptides are the analyte, the test sample, typically a biological sample, is incubated with antibodies directed against the peptide under conditions that allow the formation of antigen-antibody complexes. It may be desirable to treat the biological sample to release putative bacterial components prior to testing. Various formats can be employed. For example, a “sandwich assay” may be employed, where antibody bound to a solid support is incubated with the test sample; washed; incubated with a second, labeled antibody to the analyte, and the support is washed again. Analyte is detected by determining if the second antibody is bound to the support. In a competitive format, a test sample is usually incubated with antibody and a labeled, competing antigen is also incubated, either sequentially or simultaneously.

[0174] Also included as an embodiment of the invention is an immunoassay kit comprised of one or more peptides of the invention, or one or more antibodies to said peptides, and a buffer, packaged in suitable containers.

[0175] As used herein, a “biological sample” refers to a sample of tissue or fluid isolated from an individual, including but not limited to, for example, plasma, serum, spinal fluid, lymph fluid, the external sections of the skin, respiratory, intestinal, and genitourinary tracts, tears, saliva, milk, blood cells, tumours, organs, and also samples of in vitro cell culture constituents (including but not limited to conditioned medium resulting from the growth of cells in cell culture medium, putatively virally infected cells, recombinant cells, and cell components).

[0176] In a related diagnostic assay, the present invention provides nucleic acid probes for detecting a mycobacterial infection.

[0177] Using the polynucleotides of the present invention as a basis, oligomers of approximately 8 nucleotides or more can be prepared, either by excision from recombinant polynucleotides or synthetically, which hybridize with the mycobacterial sequences, and are useful in identification of mycobacteria.

[0178] The probes are a length which allows the detection of the induced or up-regulated sequences by hybridization. While 6-8 nucleotides may be a workable length, sequences of 10-12 nucleotides are preferred, and at least about 20 nucleotides appears optimal. These probes can be prepared using routine methods, including automated oligonucleotide synthetic methods. For use as probes, complete complementarity is desirable, though it may be unnecessary as the length of the fragment is increased.

[0179] For use of such probes as diagnostics, the biological sample to be analyzed, such as blood or serum, may be treated, if desired, to extract the nucleic acids contained therein. The resulting nucleic acid from the sample may be subjected to gel electrophoresis or other size separation techniques; alternatively, the nucleic acid sample may be dot blotted without size separation. The probes are usually labeled. Suitable labels, and methods for labeling probes are known in the art, and include, for example, radioactive labels incorporated by nick translation or kinasing, biotin, fluorescent probes, and chemiluminescent probes. The nucleic acids extracted from the sample are then treated with the labeled probe under hybridization conditions of suitable stringencies.

[0180] The probes may be made completely complementary to the virulence encoding polynucleotide. Therefore, usually high stringency conditions are desirable in order to prevent false positives. The stringency of hybridization is determined by a number of factors during hybridization and during the washing procedure, including temperature, ionic strength, length of time, and concentration of formamide.

[0181] It may be desirable to use amplification techniques in hybridization assays. Such techniques are known in the art and include, for example, the polymerase chain reaction (PCR) technique.

[0182] The probes may be packaged into diagnostic kits. Diagnostic kits include the probe DNA, which may be labeled; alternatively, the probe DNA may be unlabeled and the ingredients for labeling may be included in the kit in separate containers. The kit may also contain other suitably packaged reagents and materials needed for the particular hybridization protocol, for example, standards, as well as instructions for conducting the test.

[0183] In a preferred embodiment, a peptide (or fragment or variant or derivative) of the present invention is used in a diagnostic assay to detect the presence of a T-lymphocyte, which T-lymphocyte has been previously exposed to an antigenic component of a mycobacterial infection in a patient.

[0184] In more detail, a T-lymphocyte which has been previously exposed to a particular antigen will be activated on subsequent challenge by the same antigen. This activation provides a means for identifying a positive diagnosis of mycobacterial infection. In contrast, the same activation is not achieved by a T-lymphocyte which has not been previously exposed to the particular antigen.

[0185] The above “activation” of a T-lymphocyte is sometimes referred to as a “recall response” and may be measured, for example, by determining the release of interferon (eg. IFN-γ) from the activated T-lymphocyte. Thus, the presence of a mycobacterial infection in a patient may be determined by the release of a minimum concentration of interferon from a T-lymphocyte after a defined time period following in vitro challenge of the T-lymphocyte with a peptide (or fragment or variant or derivative) of the present invention.

[0186] In use, a biological sample containing T-lymphocytes is taken from a patient, and then challenged with a peptide (or fragment, variant, or derivative thereof) of the present invention.

[0187] The above T-lymphocyte diagnostic assay may include an antigen presenting cell (APC) expressing at least one major histocompatibility complex (MHC) class II molecule expressed by the patient in question. The APC may be inherently provided in the biological sample, or may be added exogenously. In one embodiment, the T-lymphocyte is a CD4 T-lymphocyte.

EXAMPLE 1 Generation of Putative Promoter Library

[0188] The routine molecular biology methods employed were as described in the standard reference protocols (Ausubel F. M., Brent R., Kingston R. E., Moore D. D., Seidman J. G., Smith J. A. and Struhl K. (1992). “Current protocols in molecular biology”. John Wiley & Sons, Chichester).

[0189] The promoter library was prepared by partial restriction endonuclease digestion (Sau 3A1) of M. tuberculosis H37Rv chromosomal DNA. Digested DNA was size fractionated and fragments of 1-2 kb in size recovered using the Qiaex II Gel Extraction Kit (Qiagen Ltd).

[0190] Recovered fragments were ligated into the vector pCREP8GFPTTL which had been linearised with Bgl II and dephosphorylated. The vector PCREP8GFPTTL is based upon the vector pCREP8 provided by Dr P O'Gaora, ICSM, London which is itself based upon the pNG2 replicon (Radford and Hodgson, 1991, Plasmid 25: 149-153).

[0191] Modifications of pCREP8 to create pCREP8GFPTTL include replacement of the region encoding Cre recombinase with the gene encoding GFPmut2 (Cormack, Valdivia and Falkow. Gene. 1996, 173: 33-38). In addition transcriptional terminators from CeIA (from C. thermocelum) and Ferredoxin (from C. pasteurianum) genes were inserted upstream and downstream of the GFPmut2 gene respectively. Finally translational stops were introduced in all three reading frames by insertion of a linker between the Bgl II cloning site and the ribosome binding site immediately preceding the ATG start codon of the GFPmut2 gene.

[0192] The ligation mixture was transformed into E. coli and resulting transformants banked into 96 well plates to give 23,040 individual clones. Large scale plasmid isolation was performed on pools of 480 clones using Qiagen Maxi plasmid preps (Qiagen Ltd).

EXAMPLE 2 Putative Promoters Identified by Sequence Homology

[0193] Promoter regions for targeted fusions were selected by screening the annotated M. tuberculosis genome (http://www.sanger.ac.uk/Projects/M_tuberculosis/ or http://pedant.mips.biochem.mpg.de/) for secreted proteins, surface exposed proteins and those with homology to known virulence factors or implicated previously in mycobacterial virulence using text searches.

[0194] In this way a number of candidates for targeted fusions may be isolated. Having identified a promoter, the organisation of the surrounding gene structure was examined and, where possible, a promoter was identified.

[0195] Mycobacterial promoters lack typical −35 and −10 sequences [Das Gupta S K, Bashyam M D and Tyagi A K (1993). J. Bacteriol., 175: 5186-5192].

[0196] In this instance the region immediately upstream of the gene or operon of interest was amplified by PCR using tailed primers and cloned directly into the Bgl II site of pCREP8GFPTTL. The GFPmut2 vector was used as described above using macrophage cell line J774. 1, in vitro culture grown in Middlebrook 7H9 supplemented with 10% OADC and 0.25% Triton WR1339 (synthetic mycobacterial culture medium), or DMEM.

[0197] Table 1 lists a number of such promoters. TABLE 1 FACS analysis of Targeted Promoter-GFP Fusions in Macrophage Infection Assays Net change** in % popu- Identity/Predicted function lation > Promoter Gene arrangement⁺ 10³ TF m1 Invasion loci mce1 operon Rv0167-0174 3.3 TF h sigE operon Rv1221-1224 21.7 TF m2 mce2 operon 1.46 TF t Rv2462c trigger factor 4.41 TF2 mce3 operon Rv1964-1971 12.6 TF3 probable secreted protein Rv1910c 2.9 TF7 Weak similarity to pollen antigens Rv1919c 6 TF10 Putative exported protein Rv1477-1478 40 TF11 putative exported protease Rv2671/2672/2673 5.42 TF13 proteolytic subunit Rv2461c 3.7 TF15 single gene heat shock protein Rv0384c 11.5 H37Rv Non-fluorescing control −0.1 Control

EXAMPLE 3 Protocol for Macrophage Infection, Harvesting, FACS Analysis and Sorting, and Recovery of M. tuberculosis

[0198] Macrophage infection with batch culture samples of M. tuberculosis. Wells were harvested at intervals of 24 hr, 48 hr and 72 hrs post infection.

[0199] Materials

[0200] Mouse macrophage cell line J774A.1 (obtainable from, for example, the ECACC) in 6 well plates were seeded at 5×10⁵ cells per well.

[0201] Tissue culture medium—Dulbecco's Modified Eagle Medium supplemented with 200 mM L-glutamate, 10% foetal bovine serum (gamma-irradiated) and 10 mM HEPES.

[0202] Batch culture sample of M. tuberculosis was grown to mid-late exponential log (O.D₆₀₀ 0.6-0,8).

[0203] Liquid Middlebrook 7H9 medium (Difco) supplemented with 10% OADC enrichment (Difco) and 0.25% Triton WR1339, or organisms were cultured on solid Middlebrook 7H10 medium (Difco) supplemented with 10% OADC enrichment (Difco) for growth of M. tuberculosis outside of macrophage.

[0204] Procedure

[0205] 1. Macrophage were grown until confluent (4×10⁶ cells per well).

[0206] 2. Bacterial samples were prepared using the following procedure:

[0207] 2-3 week old colonies were scraped from 7H10+OADC agar plates and resuspended in 10 mls of 7H9+OADC+Triton WR1339. A universal tube (22 mm diameter×90 mm height) containing 10 mls of 7H9+OADC+Triton WR1339 was inoculated with 500 μl of the bacterial suspension. Bacteria were grown on an orbital shaker (200 rpm) at 37° C. for 7 days

[0208] 500 μls of bacterial culture was inoculated into a universal tube (22 mm diameter×90 mm height) containing 10 mls of 7H9+OADC+Triton WR1339 1 ml. Bacteria were grown on an orbital shaker (200 rpm) at 37° C. for 5 days (O.D₆₀₀ 0.6-0.8).

[0209] Bacterial samples were diluted in DMEM to a cell density of 1×10⁷/ml—a multiplicity of approximately 2:1 (bacteria to cells) or less is preferred.

[0210] 3. Tissue culture medium was removed from each tissue culture well

[0211] 4. 1 ml of bacterial suspension was added to each well and incubated at 37° C. for 3 hours in an atmosphere of 5% CO₂ in air.

[0212] 5. The inoculum suspension and was removed and each well washed 4 times with 1×phosphate buffered saline (PBS) pre-warmed to 37° C.

[0213] 6. 3 ml fresh pre-warmed DMEM was added to each well.

[0214] 7. Infected monolayers were incubated at 37° C. in an atmosphere of 5% CO₂ in air, for a period of 1, 2 or 3 days.

[0215] 8. Wells for each sample were harvested at appropriate time points as follows:

[0216] i) Culture medium was removed by aspiration and monolayers washed with pre-warmed PBS to remove any external bacteria.

[0217] ii) The PBS buffer was removed and replaced with 1 ml of 0.25% Triton X-100 in water.

[0218] iii) The monolayers were Incubated for 25 mins before disruption of the monolayer with a pastette to release bacteria from the macrophage.

[0219] iv) Samples were transferred to a FACS tube and examined using a FACS scanner/sorter at Cat III collecting highly fluorescent bacteria (typically greater than 10³ logs of fluorescence).

[0220] 9. Bacteria were recovered by passing the sorted suspensions through a 0.2 μM filter.

[0221] 10. Recovered bacteria on the filter membrane were cultured on Middlebrook 7H10+OADC agar plates and grown at 37° C. for 2 weeks.

[0222] 11. Bacteria were scraped from the filter membrane into 10 mIs of 7H9+ADC medium and grow for 5-7 days (37° C., 200 rpm).

[0223] Notes:

[0224] i) The macrophage infection assay and sorting were repeated until the desired level of enrichment of fluorescent bacteria was attained

[0225] ii) Bacteria carrying M. tuberculosis promoters that were highly active outside of the macrophage environment were removed by culturing bacteria in Middlebrook 7H9+ADC medium then FACS sorting to collect the non-fluorescent bacteria. (This selection procedure was carried out between passage 1 and passage 2 of the repeat macrophage infection rounds).

EXAMPLE 4 Alternative Macrophage Assay Procedures

[0226] 1). Triccas, J. A. et al. (1999). Microbiology 145, 2923-2930.

[0227] Procedure

[0228] Macrophage cells were seeded at 2×10⁵ per well in 24-well plates and incubated at 37° C. in 5% CO₂ for 7 days. Macrophage monolayers were infected with bacteria at a multiplicity of infection (m.o.i) of 1:1. After 4 hours of infection extracellular bacteria were removed by washing 4× with PBS and incubation continued in 5% CO₂.

[0229] After 5-6 days of infection, infected macrophages were washed 3× in PBS, scraped into 1 ml PBS and analysed by FACS. To recover bacteria, sorted macrophages were centrifuged and lysed in water plus 0.1% Tween 80. Recovered bacteria were grown in 7H9 medium for 7 days and macrophage infection and sorting repeated until the desired level of enrichment of macrophage/fluorescent bacteria was attained.

[0230] To select clones with enhanced intracellular expression the macrophage infection was performed as above, however the macrophage were then lysed with Tween 80 to release the bacteria prior to FACS sorting.

[0231] 2). Kremer, L. et al. (1995). Mol Microbiol. 17, 913-922.

[0232] Procedure (Macrophage Infection Only)

[0233] J774A.1 macrophages were seeded in eight-chamber culture slides and incubated overnight at 37° C. in 5% CO₂. Just prior to infection, the monolayer was washed with RPM I1640. Recombinant BCG was added at a m.o.i. of 1-5 bacteria per macrophage.

[0234] After an overnight infection at 37° C. in the presence of 5% CO₂, the cells were washed 3× with RPMI to remove possible extracellular bacteria. The macrophage were then examined using a fluorescence microscope.

[0235] 3). Dhandayuthapani, S. et al. (1995). Mol. Microbiol. 17, 901-912.

[0236] Procedure

[0237] Macrophages were seeded in 100 mm tissue-culture petri dishes (5×10⁶). After overnight attachment at 37° C. in the presence of 5% CO₂ the macrophage were infected at a m.o.i of 1 bacteria per macrophage. One hour after infection, the monolayers were washed 3× with prewarmed PBS to remove non-ingested bacteria and the DMEM replaced.

[0238] The macrophages were harvested 6 days post-infection by washing with PBS and then scraped from the dish. The macrophages were collected by centrifugation and broken by 20-30 passages through a 23-gauge needle: intact cells and nuclei were pelleted and the supernatant containing bacteria collected. The bacteria were then pelleted, washed with PBS and centrifuged again. The final bacterial pellet was suspended in PBS for FACS analysis.

[0239] 4). Via, L. E. et al. (1996). J. Bacteriol. 178, 3314-3321.

[0240] Procedure

[0241] J774 macrophage monolayers were seeded at a density of 7.5×10⁶ cells per 100 mm-diameter tissue culture petri dish. After overnight attachment at 37° C. in the presence of 5% CO₂, macrophages were infected at a m.o.i of 10-20 bacteria per macrophage. One hour after infection any extracellular bacteria were removed by washing 3× with prewarmed PBS, then fresh DMEM+5% FBS added.

[0242] The medium was replaced every 3-4 days of culture. The infected macrophages were incubated for 10 mins, 3 days, 7 days and 11 days (FACS analysis was performed on the 10 min, 7 day and 11 day samples) before harvesting. At harvest the monolayers were washed 3× with PBS, scraped from the dish, centrifuged then homogenised in 20 mM HEPES (pH 7.2)−250mM sucrose. For FACS the homogenate was then subjected to three rounds of centrifugation to remove unbroken macrophage and macrophage debris, the final bacterial pellet was suspended in PBS. FACS analysis and sorting were carried out as described above in reference 3.

[0243] 5). Barker L. P. et al. (1998). Mol. Microbiol. 29, 1167-1177.

[0244] Procedure

[0245] Macrophages were seeded into tissue culture dishes at a concentration of 2×10⁵ cells/ml total volume. Macrophages were grown to semi-confluency before bacteria were added at a m.o.i. of 1-5 bacteria per macrophage. After 4 hours growth at 37° C. in the presence of 5% CO₂ the medium was removed and fresh DMEM supplemented with amikacin 100 μg/ml was added to kill extracellular organisms.

[0246] After 24 hours at 32° C. the concentration of amikacin was reduced to 20 μg/ml. At three days after infection (the point at which most phagocytic vesicles contain only one organism) the macrophages are washed in PBS, scraped from the dish and subjected to a very gentle and controlled lysis that disrupts the cell membrane without compromising the nuclear membrane.

[0247] Vesicles containing bacteria are then isolated by centrifugation, the supernatant removed and diluted with PBS for FACS analysis. Fluorescent bacterial clones that were sorted away from non-fluorescent vesicles and vesicles containing non-fluorescent organisms were screened further using a confocal microscope.

[0248] Those clones that appeared to fluoresce intracellularly but not on 7H10 agar or in tissue culture media were passaged through macrophage again. After 3-4 days of growth the bacteria were harvested from the macrophage by lysing the macrophage with 0.1% Triton-X in PBS for 5 min, after which the detergent was diluted with 9 volumes of PBS ready for FACS analysis.

EXAMPLE 5 Elucidation of Mycobacterial Nucleic Acid Coding Sequences under the Transcriptional Control of Identified Promoters

[0249] DFI allows identification of a promoter which is induced or up-regulated during infection of macrophage, a key step in the pathogenesis of tuberculosis.

[0250] Once the DNA sequence and orientation of a promoter region has been determined the exact location can be mapped by doing a DNA homology search (e.g BLASTN or BLASTX, see http://www.sanger.ac.uk/) on the published M. tuberculosis H37Rv genome to reveal the gene or operon under control of the identified promoter region.

[0251] Knockout mutants of the gene(s) under control of the identified promoter may then be prepared to see if they are essential for virulence. The fact that the genes are expressed or up-regulated during the infection means they may be essential for virulence of the organism (as demonstrated by testing a knockout mutant in a suitable model).

[0252] These data help identify a) a potential vaccine candidate which the host immune response can be targeted to; b) a gene which when inactivated sufficiently attenuates the organism that it could be considered suitable as a live vaccine; c) a target for the development of a new antibiotic.

[0253] A suitable plasmid DNA vector (Tascon R E et al., 1996 Nat. Med. 2:8 888-892; Huygen K et al., 1996 Nat. Med. 2:8 893-898) containing the DNA sequence corresponding to one or more of the genes in an identified operon may be tested as a DNA vaccine in comparison with pre-existing TB vaccines. Similarly, gene products thereof may be tested as a vaccine in a guinea pig protection model.

EXAMPLE 6 Delete One or More of the Genes from M. tuberculosis in Order to Attenuate its Virulence while Retaining Immunogenicity

[0254] One or more genes that are identified may be disrupted using allelic exchange. In brief, the gene of interest is cloned with 1-2 kb of flanking DNA either side and is inactivated by deletion of part of the coding region and insertion of an antibiotic resistance marker, such as hygromycin.

[0255] The manipulated fragment is then transferred to a suitable suicide vector eg. pPR23 and is transformed into the wild-type parent strain of M. tuberculosis. Mutants are recovered by selecting for antibiotic resistant strains. Genotypic analysis (Southern Blotting with a fragment specific to the gene of interest) is performed on the selected strains to confirm that the gene has been disrupted.

[0256] The mutant strain is then studied to determine the effect of the gene disruption on the phenotype. In order to use it as a vaccine candidate it would be necessary to demonstrate attenuated virulence. This can be done using either a guinea pig or mouse model of infection. Animals are infected with the mutant strain and the progression of disease is monitored by determining the bacterial load in different organs, in particular the lung and spleen, at specific time points post infection, typically up to 16 weeks.

[0257] Comparison is made to animals infected with the wild-type strain which should have a significantly higher bacterial load in the different organs. Long-term survival studies and histopathology can also be used to assess virulence and pathogenicity.

[0258] Once attenuated virulence has been established, protection and immunogenicity studies can be performed to assess the potential of the strain as a vaccine. Suitable references for allelic exchange and preparation of TB mutants are McKinney et al., 2000 and Pelicic et al., 1997, [1, 2].

EXAMPLE 7 Select One or More of Our Genes, which Encode Proteins that are Immunogenic, and put them into BCG or an Attenuated Strain of M. tuberculosis to Enhance its Overall Immunogenicity

[0259] The gene of interest is amplified from the M. tuberculosis genome by PCR. The amplified product is purified and cloned into a plasmid (pMV306) that integrates site specifically into the mycobacterial genome at the attachment site (attB) for mycobacteriophage L5 [3].

[0260] BCG is transformed with the plasmid by electroporation, which involves damaging the cell envelope with high voltage electrical pulses, resulting in uptake of the DNA. The plasmid integrates into the BCG chromosome at the attB site generating stable recombinants. Recombinants are selected and are checked by PCR or Southern blotting to ensure that the gene has been integrated. The recombinant strain is then used for protection studies.

EXAMPLE 8 Use Recombinant Carriers such as Attenuated Salmonella and the Vaccinia Virus to Express and Present TB Genes

[0261] One of the best examples of this type of approach is the use of Modified Vaccinia virus Ankara (MVA) [4]. The gene of interest is cloned into a vaccinia virus shuttle vector, e.g. pSC11. Baby Hamster Kidney (BHK) cells are then infected with wild-type MVA and are transfected with the recombinant shuttle vector. Recombinant virus is then selected using a suitable selection marker and viral plaques, selected and purified.

[0262] Recombinant virus is normally delivered as part of a prime-boost regime where animals are vaccinated initially with a DNA vaccine encoding the TB genes of interest under the control of a constitutive promoter. The immune response is boosted by administering recombinant MVA carrying the genes of interest to the animals at least 2 weeks later.

EXAMPLE 9 Sub-Unit Vaccines Containing a Single Peptide/Protein or a Combination of Proteins

[0263] To prepare sub-unit vaccines with one or more peptides or proteins it is first of all necessary to obtain a supply of protein or peptide to prepare the vaccine. Up to now, this has mainly been achieved in mycobacterial studies by purifying proteins of interest from TB culture. However, it is becoming more common to clone the gene of interest and produce a recombinant protein.

[0264] The coding sequence for the gene of interest is amplified by PCR with restriction sites inserted at the N terminus and C terminus to permit cloning in-frame into a protein expression vector such as pET-15b. The gene is inserted behind an inducible promoter such as lacZ. The vector is then transformed into E. coli which is grown in culture. The recombinant protein is over-expressed and is purified.

[0265] One of the common purification methods is to produce a recombinant protein with an N-terminal His-tag. The protein can then be purified on the basis of the affinity of the His-tag for metal ions on a Ni-NTA column after which the His-tag is cleaved. The purified protein is then administered to animals in a suitable adjuvant [5].

EXAMPLE 10 Plasmid DNA Vaccines Carrying One or More of the Identified Genes

[0266] DNA encoding a specific gene is amplified by PCR, purified and inserted into specialised vectors developed for vaccine development, such as pVAX1. These vectors contain promoter sequences, which direct strong expression of the introduced DNA (encoding candidate antigens) in eukaryotic cells (eg. CMV or SV40 promoters), and polyadenlyation signals (eg. SV40 or bovine growth hormone) to stabilise the mRNA transcript.

[0267] The vector is transformed into E. coli and transformants are selected using a marker, such as kanamycin resistance, encoded by the plasmid. The plasmid is then recovered from transformed colonies and is sequenced to check that the gene of interest is present and encoded properly without PCR generated mutations.

[0268] Large quantities of the plasmid is then produced in E. coli and the plasmid is recovered and purified using commercially available kits (eg. Qiagen Endofree-plasmid preparation). The vaccine is then administered to animals for example by intramuscular injection in the presence or absence of an adjuvant.

EXAMPLE 11 Preparation of DNA Expression Vectors

[0269] DNA vaccines consist of a nucleic acid sequence of the present invention cloned into a bacterial plasmid. The plasmid vector pVAX1 is commonly used in the preparation of DNA vaccines. The vector is designed to facilitate high copy number replication in E. coli and high level transient expression of the peptide of interest in most mammalian cells (for details see manufacturers protocol for pVAX1 ( catalog no. V260-20 www.invitrogen.com).

[0270] The vector contains the following elements

[0271] Human cytomegalovirus immediate-early (CMV) promoter for high-level expression in a variety of mammalian cells

[0272] T7 promoter/priming site to allow in vitro transcription in the sense orientation and sequencing through the insert

[0273] Bovine growth hormone (BGH) polyadenylation signal for efficient transcription termination and polyadenylation of mRNA

[0274] kanamycin resistance gene for selection in E. coli

[0275] A multiple cloning site

[0276] pUC origin for high-copy number replication and growth in E. coli

[0277] BGH reverse priming site to permit sequencing through the insert

[0278] Vectors may be prepared by means of standard recombinant techniques which are known in the art, for example Sambrook et al., (1989). Key stages in preparing the vaccine are as follows:

[0279] The gene of interest is ligated into pVAX1 via one of the multiple cloning sites

[0280] The ligation mixture is then transformed into a competent E. coli strain (eg. TOP10) and LB plates containing 50 μg/ml kanamycin are used to select transformants.

[0281] Clones are selected and may be sequenced to confirm the presence and orientation of the gene of interest.

[0282] Once the presence of the gene has been verified, the vector can be used to transfect a mammalian cell line to check for protein expression. Methods for transfection are known in the art and include, for example, electroporation, calcium phosphate, and lipofection.

[0283] Once peptide expression has been confirmed, large quantities of the vector can be produced and purified from the appropriate cell host, e.g. E. coli.

[0284] pVAX1 does not integrate into the host chromosome. All non-essential sequences have been removed to minimise the possibility of integration. When constructing a specific vector, a leader sequence may be included to direct secretion of the encoded protein when expressed inside the eukaryotic cell.

[0285] Other examples of vectors that have been used are V1 Jns.tPA and pCMV4 (Lefevre et al., 2000; and Vordermeier et al., 2000).

[0286] Expression vectors may be used that integrate into the genome of the host, however, it is more common and more preferable to use a vector that does not integrate. The example provided, pVAX1, does not integrate. Integration would lead to the generation of a genetically modified host which raises other issues.

EXAMPLE 12 RNA Vaccine

[0287] As discussed on page 15 of U.S. Pat. No. 5,783,386, one approach is to introduce RNA directly into the host.

[0288] Thus, the vector construct (Example 11) may be used to generate RNA in vitro and the purified RNA then injected into the host. The RNA would then serve as a template for translation in the host cell. In this embodiment. In this embodiment, integration would not occur.

[0289] Another option is to use an infectious agent such as the retroviral genome carrying RNA corresponding to the gene of interest. In this embodiment, integration into the host genome will occur.

[0290] Another option is the use of RNA replicon vaccines which can be derived from virus vectors such as Sindbis virus or Semliki Forest virus. These vaccines are self-replicating and self-limiting and may be administered as either RNA or DNA which is then transcribed into RNA replicons in vivo. The vector eventually causes lysis of the transfected cells thereby reducing concerns about integration into the host genome. Protocols for RNA vaccine construction are detailed in Cheng, et al. (2001).

EXAMPLE 13 Diagnostic Assays Based on Assessing T Cell Responses

[0291] For a diagnostic assay based on assessing T cell responses it would be sufficient to obtain a sample of blood from the patient. Mononuclear cells (monocytes, T and B lymphocytes) can be separated from the blood using density gradients such as Ficoll gradients.

[0292] Both monocytes and B-lymphocytes are both able to present antigen, although less efficiently than professional antigen presenting cells (APCs) such as dendritic cells. The latter are more localised in lymphoid tissue.

[0293] The simplest approach would be to add antigen to the separated mononuclear cells and incubate for a week and then assess the amount of proliferation. If the individual had been exposed to the antigen previously through infection, then T-cell closes specific to the antigen should be more prevalent in the sample and should respond.

[0294] It is also possible to separate the different cellular populations should it be desired to control the ratio of T cells to APC's.

[0295] Another variation of this type of assay is to measure cytokine production by the responding lymphocytes as a measure of response. The ELISPOT assay described below in Example 14 is a suitable example of this variation.

EXAMPLE 14 Detection of Latent Mycobacteria

[0296] A major problem for the control of tuberculosis is the presence of a large reservoir of asymptomatic individuals infected with tubercle bacilli. Dormant bacilli are more resistant to front-line drugs.

[0297] The presence of latent mycobacteria-associated antigen may be detected indirectly either by detecting antigen specific antibody or T-cells in blood samples.

[0298] The following method is based on the method described in Lalvani et al. (2001) in which a secreted antigen, ESAT-6, was identified as being expressed by members of the M. tuberculosis complex but is absent from M. bovis BCG vaccine strains and most environmental mycobacteria. 60-80% of patients also have a strong cellular immune response to ESAT-6. An ex-vivo ELISPOT assay was used to detect ESAT-6 specific T cells.

[0299] As applied to the present invention:

[0300] A 96 well plate is coated with cytokine (eg. interferon-(, IL-2)-specific antibody. Peripheral blood monocytes are then isolated from patient whole blood and are applied to the wells.

[0301] Antigen (ie. one of the peptides, fragments, derivatives or variants of the present invention) is added to stimulate specific T cells that may be present and the plates are incubated for 24 h. The antigen stimulates cytokine production which then binds to the specific antibody.

[0302] The plates are washed leaving a footprint where antigen-specific T cells were present.

[0303] A second antibody coupled with a suitable detection system, eg. enzyme, is then added and the number of spots are enumerated after the appropriate substrate has been added.

[0304] The number of spots, each corresponding to a single antigen-specific T cell, is related to the total number of cells originally added.

[0305] The above Example also describes use of an antigen that may be used to distinguish. TB infected individuals from BCG vaccinated individuals. This could be used in a more discriminative diagnostic assay.

[0306] The following Table 2 lists the preferred promoters, peptides, and corresponding DNA coding sequences of the present invention. TABLE 2 amino acid nucleic acid name sequence sequence Mce1 operon promoter 1 Rv0167 2 3 Rv0168 4 5 Rv0169 6 7 Rv0170 8 9 Rv0171 10 11 Rv0172 12 13 Rv0173 14 15 Rv0174 16 17 Rv0175 117 118 Mce2 operon promoter 18 Rv0586 19 20 Rv0587 21 22 Rv0588 23 24 Rv0589 25 26 Rv0590 27 28 Rv0591 29 30 Rv0592 31 32 Rv0593 33 34 Rv0594 35 36 Mce3 operon promoter 37 Rv1964 38 39 Rv1965 40 41 Rv1966 42 43 Rv1967 44 45 Rv1968 46 47 Rv1969 48 49 Rv1970 50 51 Rv1971 52 53 Rv2462c promoter 54 Rv2462c 55 56 SigE/htrA operon promoter 57 Ry1221 58 59 Rv1222 60 61 Rv1223 62 63 Rv1224 64 65 Rv1477/1478 operon promoter 66 Rv1477 67 68 Rv1478 69 70 Rv1919c promoter 71 Rv1919c 72 73 Rv0384c promoter 74 Rv0384c 75 76 Rv2671-2672-2673 promoter 77 Rv2671 78 79 Rv2672 80 81 Rv2673 82 83 Rv1909/1910/1912c promoter 84 Rv1910c 85 86 Rv1911c 87 88 Rv1912c 89 90 Rv2461c/2460c promoter 91 Rv2461c 92 93 Rv2460c 94 95 Rv1179c promoter 96 Rv1179c 97 98 Rv1646 promoter 99 Rv1646 100 101 Rv2042c (Rv2043- 102 2037c) promoter Rv2037c 103 104 Rv2038c 105 106 Rv2039c 107 108 Rv2040c 109 110 Rv2041c 111 112 Rv2042c 113 114 Rv2043c 115 116

[0307] References:

[0308] 1. McKinney, J. D., et al., Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase [see comments]. Nature, 2000. 406(6797): p. 735-8.

[0309] 2. Pelicic, V., et al., Efficient allelic exchange and transposon mutagenesis in Mycobacterium tuberculosis. Proc Natl Acad Sci USA, 1997. 94(20): p. 10955-60.

[0310] 3. Lee, M. H., et al., Site-specific integration of mycobacteriophage L5: integration-proficient vectors for Mycobacterium smegmatis, Mycobacterium tuberculosis, and bacille Calmette-Guerin. Proc Natl Acad Sci USA, 1991. 88(8): p. 3111-5.

[0311] 4. McShane, H., et al., Enhanced immunogenicity of CD4(+) t-cell responses and protective efficacy of a DNA-modified vaccinia virus Ankara prime-boost vaccination regimen for murine tuberculosis. Infect Immun, 2001. 69(2): p. 681-6.

[0312] 5. Movahedzadeh, F., M. J. Colston, and E. O. Davis, Characterization of Mycobacterium tuberculosis LexA: recognition of a Cheo (Bacillus-type SOS) box. Microbiology, 1997. 143(Pt 3): p. 929-36.

[0313] Additional References:

[0314] Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbour Laboratory Press, Cold Spring Harbour, N.Y.

[0315] Lefever, P., O. Denis, L. De Wit, A. Tanghe, P. Vandenbussche, J. Content, and K. Huygen. 2000. Cloning of the gene encoding a 22-kilodalton cell surface antigen of Mycobacterium bovis BCG and analysis of its potential for DNA vaccination against tuberculosis. Infection and Immunity. 68:1040-1047.

[0316] Vordermeier, H. M., P. J. Cockle, A. O. Whelan, S. Rhodes, M. A. Chambers, D. Clifford, K. Huygen, R. Tascon, D. Lowrie, M. J. Colston, and R. G.

[0317] Hewinson. 2000. Effective DNA vaccination of cattle with the mycobacterial antigens MPB83 and MPB70 does not compromise the specificity of the comparative intradermal tuberculin skin test. Vaccine. 19:1246-1255.

[0318] Cheng, W., C. Hung, C. Chai, K. Hsu, L. He, C. Rice, M. Ling, and T. Wu. 2001. Enhancement of Sindbis virus self-replicating RNA vaccine potency by linkage of Mycobacterium tuberculosis heat shock protein 70 gene to an antigen. J. Immunol. 166:6218-6226.

[0319] Lalvani, A. et al., 2001. Enhanced contact tracing and spatial tracking of Mycobacterium tuberculosis infection by enumeration of antigen-specific T cells. The Lancet 357:2017-2021.

1 118 1 330 DNA Mycobacterium tuberculosis 1 ggtgctcaag actgaactgc gattgcgcta cggcgcctgt gtgaatgttg aaagacgttc 60 tgcatcagct ggtttcacgg agagaaggga aaaccgacag aaattgtaac gtttgcccgc 120 tattgacgaa gggttaaatg tgcggatgcc ttacactcct ggctggccat cgggtagatt 180 cctgtggtct ccgttactcc ctgtgagtaa cgaggtggcg gtcacacacc aagggtcggg 240 gcaaggagga ggcgtgcgac atgatgcgcc gcggcgccgc gatacccagg tcggcggctt 300 gagggagccg cggtgacgac gtcgacaacg 330 2 265 PRT Mycobacterium tuberculosis 2 Val Thr Thr Ser Thr Thr Leu Gly Gly Tyr Val Arg Asp Gln Leu Gln 1 5 10 15 Thr Pro Leu Thr Leu Val Gly Gly Phe Phe Arg Met Cys Val Leu Thr 20 25 30 Gly Lys Ala Leu Phe Arg Trp Pro Phe Gln Trp Arg Glu Phe Ile Leu 35 40 45 Gln Cys Trp Phe Ile Met Arg Val Gly Phe Leu Pro Thr Ile Met Val 50 55 60 Ser Ile Pro Leu Thr Val Leu Leu Ile Phe Thr Leu Asn Ile Leu Leu 65 70 75 80 Ala Gln Phe Gly Ala Ala Asp Ile Ser Gly Ser Gly Ala Ala Ile Gly 85 90 95 Ala Val Thr Gln Leu Gly Pro Leu Thr Thr Val Leu Val Val Ala Gly 100 105 110 Ala Gly Ser Thr Ala Ile Cys Ala Asp Leu Gly Ala Arg Thr Ile Arg 115 120 125 Glu Glu Ile Asp Ala Met Glu Val Leu Gly Ile Asp Pro Ile His Arg 130 135 140 Leu Val Val Pro Arg Val Leu Ala Ser Met Leu Val Ala Thr Leu Leu 145 150 155 160 Asn Gly Leu Val Ile Thr Val Gly Leu Val Gly Gly Phe Leu Phe Gly 165 170 175 Val Tyr Leu Gln Asn Val Ser Gly Gly Ala Tyr Leu Ala Thr Leu Thr 180 185 190 Leu Ile Thr Gly Leu Pro Glu Val Val Ile Ala Thr Ile Lys Ala Ala 195 200 205 Thr Phe Gly Leu Ile Ala Gly Leu Val Gly Cys Tyr Arg Gly Leu Thr 210 215 220 Val Arg Gly Gly Ser Lys Gly Leu Gly Thr Ala Val Asn Glu Thr Val 225 230 235 240 Val Leu Cys Val Ile Ala Leu Phe Ala Val Asn Val Ile Leu Thr Thr 245 250 255 Ile Gly Val Arg Phe Gly Thr Gly Arg 260 265 3 795 DNA Mycobacterium tuberculosis 3 gtgacgacgt cgacaacgct tggcggttac gtccgcgacc aactgcaaac cccgctgacc 60 ctcgtcggtg gattctttcg catgtgtgtg ctgactggaa aggcgctgtt tcgctggccg 120 ttccagtggc gcgagttcat tctgcagtgc tggttcatca tgcgggtcgg atttttaccg 180 acgatcatgg tctcgatacc gctgacggtg ctgttgatct tcacgctcaa tattctgctg 240 gcccagttcg gcgcggcaga catctccggt tccggcgcgg cgatcggcgc ggtcacccag 300 cttggcccgc tgacaacggt gctggtggtc gccggcgccg gatccacggc catctgcgcc 360 gacctgggtg cccgcaccat ccgcgaggaa atcgacgcga tggaggtgct gggcatcgat 420 cccatccacc gtctggtggt gccgcgggtg ctcgcctcga tgctggtcgc cacgctgctc 480 aacggcttgg tgatcaccgt cggcctggtc ggtggctttc tcttcggtgt ctatctgcag 540 aacgtttcgg gcggcgccta ccttgccacg ctgaccttga tcaccggcct gcccgaggtg 600 gtcatcgcaa ccatcaaagc cgcaacgttc ggcctgatcg cgggccttgt cggctgctat 660 cgggggctga ccgtccgtgg cggttccaag ggtcttggca ccgccgtcaa cgagaccgtg 720 gtgctgtgtg tgattgccct gttcgccgtc aacgtgatct tgacgaccat cggtgtgcga 780 ttcgggacgg ggcgc 795 4 289 PRT Mycobacterium tuberculosis 4 Met Ser Thr Ala Ala Val Leu Arg Ala Arg Phe Pro Arg Ala Val Ala 1 5 10 15 Asn Leu Arg Gln Tyr Gly Gly Ala Ala Ala Arg Gly Leu Asp Glu Ala 20 25 30 Gly Gln Leu Thr Trp Phe Ala Leu Thr Ser Ile Gly Gln Ile Ala His 35 40 45 Ala Leu Arg Tyr Tyr Arg Lys Glu Thr Leu Arg Leu Ile Ala Gln Ile 50 55 60 Gly Met Gly Thr Gly Ala Met Ala Val Val Gly Gly Thr Val Ala Ile 65 70 75 80 Val Gly Phe Val Thr Leu Ser Gly Ser Ser Leu Val Ala Ile Gln Gly 85 90 95 Phe Ala Ser Leu Gly Asn Ile Gly Val Glu Ala Phe Thr Gly Phe Phe 100 105 110 Ala Ala Leu Ile Asn Val Arg Ile Ala Gly Pro Val Val Thr Gly Val 115 120 125 Ala Leu Ala Ala Thr Val Gly Ala Gly Ala Thr Ala Glu Leu Gly Ala 130 135 140 Met Arg Ile Ser Glu Glu Ile Asp Ala Leu Glu Val Met Gly Ile Lys 145 150 155 160 Ser Ile Ser Phe Leu Ala Ser Thr Arg Ile Met Ala Gly Leu Val Val 165 170 175 Ile Ile Pro Leu Tyr Ala Leu Ala Met Ile Met Ser Phe Leu Ser Pro 180 185 190 Gln Ile Thr Thr Thr Val Leu Tyr Gly Gln Ser Asn Gly Thr Tyr Glu 195 200 205 His Tyr Phe Gln Thr Phe Leu Arg Pro Asp Asp Val Phe Trp Ser Phe 210 215 220 Leu Glu Ala Leu Ile Ile Thr Ala Ile Val Met Val Ser His Cys Tyr 225 230 235 240 Tyr Gly Tyr Ala Ala Gly Gly Gly Pro Val Gly Val Gly Glu Ala Val 245 250 255 Gly Arg Ser Met Arg Phe Ser Leu Val Ser Val Gln Val Val Val Leu 260 265 270 Phe Ala Ala Leu Ala Leu Tyr Gly Val Asp Pro Asn Phe Asn Leu Thr 275 280 285 Val 5 867 DNA Mycobacterium tuberculosis 5 atgtcgaccg ctgctgtgct gcgcgcccgc ttcccgcggg cggtcgccaa ccttcgtcaa 60 tatggaggtg cggcggcccg tggattggac gaggccggcc agctcacctg gttcgctttg 120 accagcatcg ggcagatcgc gcacgcgctg cgctactacc gcaaggagac gctgcggctg 180 atcgcccaga tcggcatggg taccggcgcg atggccgtcg tcggcggcac ggtcgccatc 240 gttggctttg tcacgctgtc cggcagctcg ctggtcgcaa tccagggctt cgcgtcgctg 300 ggcaacatcg gtgtcgaggc gttcaccggg ttcttcgccg cactgatcaa cgtgcgcatc 360 gccggcccag ttgtcacggg tgtcgccctg gcggccacgg tcggtgcggg tgctacggcc 420 gagctgggcg cgatgcggat cagcgaggag atcgatgccc tggaagtgat gggcatcaag 480 tcgatctcgt ttctggcctc cacccggatc atggccgggc tggtggtgat catcccgctg 540 tacgcgttgg cgatgattat gtcgttcctg tccccgcaga tcaccaccac ggtgctctac 600 gggcagtcga acggcaccta cgagcattac tttcaaacgt tcctgcgtcc cgacgatgtc 660 ttttggtcct tcttggaggc cctcatcatc actgcgatcg tcatggtcag ccactgctac 720 tacgggtacg ccgccggtgg aggccccgtc ggtgtcggcg aggccgtcgg ccgatcgatg 780 cgtttctcgt tggtctcggt gcaggtcgtt gtcctgtttg cagcgttggc gctctacggt 840 gtcgacccga acttcaatct cacggtg 867 6 454 PRT Mycobacterium tuberculosis 6 Met Thr Thr Pro Gly Lys Leu Asn Lys Ala Arg Val Pro Pro Tyr Lys 1 5 10 15 Thr Ala Gly Leu Gly Leu Val Leu Val Phe Ala Leu Val Val Ala Leu 20 25 30 Val Tyr Leu Gln Phe Arg Gly Glu Phe Thr Pro Lys Thr Gln Leu Thr 35 40 45 Met Leu Ser Ala Arg Ala Gly Leu Val Met Asp Pro Gly Ser Lys Val 50 55 60 Thr Tyr Asn Gly Val Glu Ile Gly Arg Val Asp Thr Ile Ser Glu Val 65 70 75 80 Thr Arg Asp Gly Glu Ser Ala Ala Lys Phe Ile Leu Asp Val Asp Pro 85 90 95 Arg Tyr Ile His Leu Ile Pro Ala Asn Val Asn Ala Asp Ile Lys Ala 100 105 110 Thr Thr Val Phe Gly Gly Lys Tyr Val Ser Leu Thr Thr Pro Lys Asn 115 120 125 Pro Thr Lys Arg Arg Ile Thr Pro Lys Asp Val Ile Asp Val Arg Ser 130 135 140 Val Thr Thr Glu Ile Asn Thr Leu Phe Gln Thr Leu Thr Ser Ile Ala 145 150 155 160 Glu Lys Val Asp Pro Val Lys Leu Asn Leu Thr Leu Ser Ala Ala Ala 165 170 175 Glu Ala Leu Thr Gly Leu Gly Asp Lys Phe Gly Glu Ser Ile Val Asn 180 185 190 Ala Asn Thr Val Leu Asp Asp Leu Asn Ser Arg Met Pro Gln Ser Arg 195 200 205 His Asp Ile Gln Gln Leu Ala Ala Leu Gly Asp Val Tyr Ala Asp Ala 210 215 220 Ala Pro Asp Leu Phe Asp Phe Leu Asp Ser Ser Val Thr Thr Ala Arg 225 230 235 240 Thr Ile Asn Ala Gln Gln Ala Glu Leu Asp Ser Ala Leu Leu Ala Ala 245 250 255 Ala Gly Phe Gly Asn Thr Thr Ala Asp Val Phe Asp Arg Gly Gly Pro 260 265 270 Tyr Leu Gln Arg Gly Val Ala Asp Leu Val Pro Thr Ala Thr Leu Leu 275 280 285 Asp Thr Tyr Ser Pro Glu Leu Phe Cys Thr Ile Arg Asn Phe Tyr Asp 290 295 300 Ala Asp Pro Leu Ala Lys Ala Ala Ser Gly Gly Gly Asn Gly Tyr Ser 305 310 315 320 Leu Arg Thr Asn Ser Glu Ile Leu Ser Gly Ile Gly Ile Ser Leu Leu 325 330 335 Ser Pro Leu Ala Leu Ala Thr Asn Gly Ala Ala Ile Gly Ile Gly Leu 340 345 350 Val Ala Gly Leu Ile Ala Pro Pro Leu Ala Val Ala Ala Asn Leu Ala 355 360 365 Gly Ala Leu Pro Gly Ile Val Gly Gly Ala Pro Asn Pro Tyr Thr Tyr 370 375 380 Pro Glu Asn Leu Pro Arg Val Asn Ala Arg Gly Gly Pro Gly Gly Ala 385 390 395 400 Pro Gly Cys Trp Gln Pro Ile Thr Arg Asp Leu Trp Pro Ala Pro Tyr 405 410 415 Leu Val Met Asp Thr Gly Ala Ser Leu Ala Pro Tyr Asn His Met Glu 420 425 430 Val Gly Ser Pro Tyr Ala Val Glu Tyr Val Trp Gly Arg Gln Val Gly 435 440 445 Asp Asn Thr Ile Asn Pro 450 7 1362 DNA Mycobacterium tuberculosis 7 atgacgacgc cggggaagct gaacaaggcg cgagtgccgc cctacaagac ggcgggtttg 60 ggtctagtgc tggtcttcgc gctcgtagtt gccttggtat acctgcagtt tcgcggggag 120 ttcacgccca agacgcagtt gacgatgctg tccgctcgtg cgggtttggt gatggatccc 180 gggtcgaagg tcacctataa cggggtggag atcgggcggg tagacaccat ctcggaggtc 240 acacgtgacg gcgagtcggc ggccaagttc atcttggatg tggatccgcg ttacatccac 300 ctgattccgg caaatgtgaa cgccgacatc aaggcgacca cggtgttcgg cggtaagtat 360 gtgtcgttga ccacgccgaa aaacccgaca aagaggcgga taacgccaaa agacgtcatc 420 gacgtacggt cggtgaccac cgagatcaac acgttgttcc agacgctcac ctcgatcgcc 480 8 346 PRT Mycobacterium tuberculosis 8 Met Lys Ile Thr Gly Thr Val Val Lys Leu Gly Ile Val Ser Val Val 1 5 10 15 Leu Leu Phe Phe Thr Val Met Ile Ile Val Ile Phe Gly Gln Met Arg 20 25 30 Phe Asp Arg Thr Asn Gly Tyr Thr Ala Glu Phe Ser Asn Val Ser Gly 35 40 45 Leu Arg Gln Gly Gln Phe Val Arg Ala Ser Gly Val Glu Ile Gly Lys 50 55 60 Val Lys Ala Leu His Leu Val Asp Gly Gly Arg Arg Val Arg Val Glu 65 70 75 80 Phe Asn Ile Asp Arg Ser Val Pro Leu Tyr Gln Ser Thr Thr Ala Gln 85 90 95 Ile Arg Tyr Ser Asp Leu Ile Gly Asn Arg Tyr Val Glu Leu Lys Arg 100 105 110 Gly Glu Gly Lys Gly Ala Asn Asp Leu Leu Pro Pro Gly Gly Leu Ile 115 120 125 Pro Leu Ser Arg Thr Ser Pro Ala Leu Asp Leu Asp Ala Leu Ile Gly 130 135 140 Gly Phe Lys Pro Val Phe Arg Ala Leu Asp Pro Ala Lys Val Asn Asn 145 150 155 160 Ile Ala Asn Ala Leu Ile Thr Val Phe Gln Gly Gln Gly Gly Thr Ile 165 170 175 Asn Asp Ile Leu Asp Gln Thr Ala Gln Leu Thr Ser Gln Ile Ala Glu 180 185 190 Arg Asp Gln Ala Ile Gly Glu Val Val Lys Asn Leu Asn Ile Val Leu 195 200 205 Asp Thr Thr Val Lys His Arg Lys Glu Phe Asp Glu Thr Val Asn Asn 210 215 220 Leu Glu Asn Leu Ile Thr Gly Leu Arg Asn His Ser Asp Gln Leu Ala 225 230 235 240 Gly Gly Leu Ala His Ile Ser Asn Gly Ala Gly Thr Val Ala Asp Leu 245 250 255 Leu Ala Glu Asn Arg Thr Leu Val Arg Lys Ala Val Ser Tyr Leu Asp 260 265 270 Ala Ile Gln Gln Pro Val Ile Asp Gln Arg Val Glu Leu Asp Asp Leu 275 280 285 Leu His Lys Thr Pro Thr Ala Leu Thr Ala Leu Gly Arg Ala Asn Gly 290 295 300 Thr Tyr Gly Asp Phe Gln Asn Phe Tyr Leu Cys Asp Leu Gln Ile Lys 305 310 315 320 Trp Asn Gly Phe Gln Ala Gly Gly Pro Val Arg Thr Val Lys Leu Phe 325 330 335 Ser Gln Pro Thr Gly Arg Cys Thr Pro Gln 340 345 9 1038 DNA Mycobacterium tuberculosis 9 atgaaaatca ctggaaccgt cgtcaaactc ggcatcgtct cggtggtgct gctgttcttc 60 acggtgatga tcatcgtgat tttcggtcag atgcgcttcg accggactaa tggctatacc 120 gcggagttca gcaatgtcag cgggctgcgc caaggccagt ttgtccgtgc ttcgggggta 180 gagatcggca aggtcaaagc actacacctg gtcgacggtg gccgtcgggt tcgggtggag 240 ttcaatatcg atcgttcggt gccgttgtat cagtccacga ccgcccagat ccgctattcc 300 gacctgatcg gtaaccggta cgtggagctc aaacggggtg agggcaaggg ggccaacgat 360 ctgctgccgc caggtggact catcccattg tcccgcacgt caccggcctt ggatctggac 420 gcgttgatcg gtggtttcaa gccggtgttt cgggcgttgg atcccgcgaa ggtgaacaac 480 atcgccaacg cgctcatcac cgtcttccag gggcaaggtg gcaccataaa cgacatcctc 540 gaccagaccg cgcaactgac cagccagatc gcggagcgcg atcaggcgat cggtgaggtt 600 gtcaagaacc tgaacatcgt gctggacacc acggtcaagc atcgaaaaga gttcgacgag 660 acggtcaata acttggagaa tctgatcact gggctgagga accactccga ccagttggcc 720 ggcggcctcg cgcacatcag caacggcgcc ggcacggtgg ccgacctgct tgccgagaat 780 cgcacgttgg tgcgcaaggc cgtcagctac ctggacgcta ttcagcaacc ggtcatcgac 840 cagcgcgtcg agttggacga cctgctccac aagacgccga ccgcgttgac ggcgctcgga 900 cgcgccaacg gaacctacgg cgatttccag aacttctacc tctgcgacct ccagatcaag 960 tggaacggat tccaagccgg agggccggtc cgcacggtga agctctttag ccagccgacg 1020 ggtaggtgca cgccgcaa 1038 10 515 PRT Mycobacterium tuberculosis 10 Met Arg Thr Leu Glu Pro Pro Asn Arg Met Arg Ile Gly Leu Met Gly 1 5 10 15 Ile Val Val Ala Leu Leu Val Val Ala Val Gly Gln Ser Phe Thr Ser 20 25 30 Val Pro Met Leu Phe Ala Lys Pro Ser Tyr Tyr Gly Gln Phe Thr Asp 35 40 45 Ser Gly Gly Leu His Lys Gly Asp Arg Val Arg Ile Ala Gly Leu Gly 50 55 60 Val Gly Thr Val Glu Gly Leu Lys Ile Asp Gly Asp His Ile Val Val 65 70 75 80 Lys Phe Ser Ile Gly Thr Asn Thr Ile Gly Thr Glu Ser Arg Leu Ala 85 90 95 Ile Arg Thr Asp Thr Ile Leu Gly Arg Lys Val Leu Glu Ile Glu Pro 100 105 110 Arg Gly Ala Gln Ala Leu Pro Pro Gly Gly Val Leu Pro Val Gly Gln 115 120 125 Ser Thr Thr Pro Tyr Gln Ile Tyr Asp Ala Phe Phe Asp Val Thr Lys 130 135 140 Ala Ala Ser Gly Trp Asp Ile Glu Thr Val Lys Arg Ser Leu Asn Val 145 150 155 160 Leu Ser Glu Thr Val Asp Gln Thr Tyr Pro His Leu Ser Ala Ala Leu 165 170 175 Asp Gly Val Ala Lys Phe Ser Asp Thr Ile Gly Lys Arg Asp Glu Gln 180 185 190 Ile Thr His Leu Leu Ala Gln Ala Asn Gln Val Ala Ser Ile Leu Gly 195 200 205 Asp Arg Ser Glu Gln Val Asp Arg Leu Leu Val Asn Ala Lys Thr Leu 210 215 220 Ile Ala Ala Phe Asn Glu Arg Gly Arg Ala Val Asp Ala Leu Leu Gly 225 230 235 240 Asn Ile Ser Ala Phe Ser Ala Gln Val Gln Asn Leu Ile Asn Asp Asn 245 250 255 Pro Asn Leu Asn His Val Leu Glu Gln Leu Arg Ile Leu Thr Asp Leu 260 265 270 Leu Val Asp Arg Lys Glu Asp Leu Ala Glu Thr Leu Thr Ile Leu Gly 275 280 285 Arg Phe Ser Ala Ser Phe Gly Glu Thr Phe Ala Ser Gly Pro Tyr Phe 290 295 300 Lys Val Leu Leu Ala Asn Leu Val Pro Gly Gln Ile Leu Gln Pro Phe 305 310 315 320 Val Asp Ala Ala Phe Lys Lys Arg Gly Ile Ser Pro Glu Asp Phe Trp 325 330 335 Arg Ser Ala Gly Leu Pro Ala Tyr Arg Trp Pro Asp Pro Asn Gly Thr 340 345 350 Arg Phe Pro Asn Gly Ala Pro Pro Pro Pro Pro Pro Val Leu Glu Gly 355 360 365 Thr Pro Glu His Pro Gly Pro Ala Val Pro Pro Gly Ser Pro Cys Ser 370 375 380 Tyr Thr Pro Pro Ala Asp Gly Leu Pro Arg Pro Trp Asp Pro Leu Pro 385 390 395 400 Cys Ala Asn Leu Thr Gln Gly Pro Phe Gly Gly Pro Asp Phe Pro Ala 405 410 415 Pro Leu Asp Val Ala Thr Ser Pro Pro Asn Pro Asp Gly Pro Pro Pro 420 425 430 Ala Pro Gly Leu Pro Ile Ala Gly Arg Pro Gly Glu Val Pro Pro Asn 435 440 445 Val Pro Gly Thr Pro Val Pro Ile Pro Gln Glu Ala Pro Pro Gly Ala 450 455 460 Arg Thr Leu Pro Leu Gly Pro Ala Pro Gly Pro Ala Pro Pro Pro Ala 465 470 475 480 Ala Pro Gly Pro Pro Ala Pro Pro Gly Pro Gly Pro Gln Leu Pro Ala 485 490 495 Pro Phe Ile Asn Pro Gly Gly Thr Gly Gly Ser Gly Val Thr Gly Gly 500 505 510 Ser Glu Asn 515 11 1545 DNA Mycobacterium tuberculosis 11 atgagaacgc tggaaccacc caaccgaatg cgaattgggc tcatgggcat cgtcgttgcg 60 ctgctcgttg tcgctgtggg ccaaagcttt accagtgttc ccatgctatt cgcaaagccg 120 agctactacg gccagttcac cgactccggc ggactgcaca agggcgacag ggtacgcatc 180 gccggcttgg gagtgggcac cgtggagggg ctcaagatcg acggcgacca catcgtggtc 240 aagttctcca tcggcaccaa caccatcggc accgagagcc gcctagccat ccgcaccgac 300 accatcctgg gtaggaaagt gctcgagatc gagccgcgcg gcgcccaagc gttgccgccc 360 gggggcgttt tgccggttgg gcaaagcacc accccgtacc agatttacga cgcgttcttc 420 gacgtcacca aggccgcatc cggctgggac atcgagacgg tcaagcggtc gctgaatgtg 480 ttgtcggaga ccgttgatca gacctatccg cacctgagcg ccgccctcga cggggtggct 540 aagttctccg acaccatcgg caagcgcgac gagcagatca cgcacctact agcccaggcc 600 aaccaggtgg ccagcatcct gggtgatcgc agtgagcagg tcgaccgcct attggtcaac 660 gctaagaccc tgatcgccgc gttcaacgag cgcggccgcg cggtcgacgc cctgctgggg 720 aacatctccg ctttctcggc ccaggtgcaa aaccttatca acgacaaccc gaacctgaac 780 catgtgctcg agcagctgcg catcctcacc gacctgttgg tcgaccgcaa ggaggatttg 840 gctgaaaccc tgacgatctt gggcagattc agcgcgtcgt tcggtgagac gtttgcctct 900 gggccctact tcaaagtgct gctggccaac ctggtgccgg gtcagatctt gcagccgttt 960 gtcgatgcgg cattcaagaa gcgtggtatt agcccggagg acttctggcg cagcgccggg 1020 ctgccggcat accggtggcc cgaccccaat ggcacccggt tccccaacgg tgcgccgccg 1080 ccaccaccgc cggtgttgga gggcacgccc gagcatcccg ggccggcggt gccgccggga 1140 tcgccgtgct cctacacccc gccggcggac ggtctgccgc ggccgtggga tccgctgccc 1200 tgcgctaacc tcactcaagg tccattcggt ggccccgatt tcccggcgcc gctggatgtc 1260 gcgacgtcgc cgccgaaccc agacggtcca ccgcccgccc cgggcctacc aatcgcggga 1320 cgtccgggtg aggtgccgcc gaacgttccc ggcacgccgg tgccgattcc acaggaggct 1380 ccccccgggg cacgcacgct gcccctcggg ccggcgcctg gtccggctcc gcccccggcg 1440 gcgccaggcc cgccggcacc accgggcccc gggccgcagt tgccggcccc gttcatcaac 1500 cccggcggca ccggcggtag tggcgtgacg ggaggtagcg agaat 1545 12 530 PRT Mycobacterium tuberculosis 12 Leu Ser Thr Ile Phe Asp Ile Arg Asn Leu Arg Leu Pro Gln Leu Ser 1 5 10 15 Arg Ala Ser Val Val Ile Gly Ser Leu Val Val Val Leu Ala Leu Ala 20 25 30 Ala Gly Ile Val Gly Val Arg Leu Tyr Gln Lys Leu Thr Asn Asn Thr 35 40 45 Val Val Ala Tyr Phe Thr Gln Ala Asn Ala Leu Tyr Val Gly Asp Lys 50 55 60 Val Gln Ile Met Gly Leu Pro Val Gly Ser Ile Asp Lys Ile Glu Pro 65 70 75 80 Ala Gly Asp Lys Met Lys Val Thr Phe His Tyr Gln Asn Lys Tyr Lys 85 90 95 Val Pro Ala Asn Ala Ser Ala Val Ile Leu Asn Pro Thr Leu Val Ala 100 105 110 Ser Arg Asn Ile Gln Leu Glu Pro Pro Tyr Arg Gly Gly Pro Val Leu 115 120 125 Ala Asp Asn Ala Val Ile Pro Val Glu Arg Thr Gln Val Pro Thr Glu 130 135 140 Trp Asp Glu Leu Arg Asp Ser Val Ser His Ile Ile Asp Glu Leu Gly 145 150 155 160 Pro Thr Pro Glu Gln Pro Lys Gly Pro Phe Gly Glu Val Ile Glu Ala 165 170 175 Phe Ala Asp Gly Leu Ala Gly Lys Gly Lys Gln Ile Asn Thr Thr Leu 180 185 190 Asn Ser Leu Ser Gln Ala Leu Asn Ala Leu Asn Glu Gly Arg Gly Asp 195 200 205 Phe Phe Ala Val Val Arg Ser Leu Ala Leu Phe Val Asn Ala Leu His 210 215 220 Gln Asp Asp Gln Gln Phe Val Ala Leu Asn Lys Asn Leu Ala Glu Phe 225 230 235 240 Thr Asp Arg Leu Thr His Ser Asp Ala Asp Leu Ser Asn Ala Ile Gln 245 250 255 Gln Phe Asp Ser Leu Leu Ala Val Ala Arg Pro Phe Phe Ala Lys Asn 260 265 270 Arg Glu Val Leu Thr His Asp Val Asn Asn Leu Ala Thr Val Thr Thr 275 280 285 Thr Leu Leu Gln Pro Asp Pro Leu Asp Gly Leu Glu Thr Val Leu His 290 295 300 Ile Phe Pro Thr Leu Ala Ala Asn Ile Asn Gln Leu Tyr His Pro Thr 305 310 315 320 His Gly Gly Val Val Ser Leu Ser Ala Phe Thr Asn Phe Ala Asn Pro 325 330 335 Met Glu Phe Ile Cys Ser Ser Ile Gln Ala Gly Ser Arg Leu Gly Tyr 340 345 350 Gln Glu Ser Ala Glu Leu Cys Ala Gln Tyr Leu Ala Pro Val Leu Asp 355 360 365 Ala Ile Lys Phe Asn Tyr Phe Pro Phe Gly Leu Asn Val Ala Ser Thr 370 375 380 Ala Ser Thr Leu Pro Lys Glu Ile Ala Tyr Ser Glu Pro Arg Leu Gln 385 390 395 400 Pro Pro Asn Gly Tyr Lys Asp Thr Thr Val Pro Gly Ile Trp Val Pro 405 410 415 Asp Thr Pro Leu Ser His Arg Asn Thr Gln Pro Gly Trp Val Val Ala 420 425 430 Pro Gly Met Gln Gly Val Gln Val Gly Pro Ile Thr Gln Gly Leu Leu 435 440 445 Thr Pro Glu Ser Leu Ala Glu Leu Met Gly Gly Pro Asp Ile Ala Pro 450 455 460 Pro Ser Ser Gly Leu Gln Thr Pro Pro Gly Pro Pro Asn Ala Tyr Asp 465 470 475 480 Glu Tyr Pro Val Leu Pro Pro Ile Gly Leu Gln Ala Pro Gln Val Pro 485 490 495 Ile Pro Pro Pro Pro Pro Gly Pro Asp Val Ile Pro Gly Pro Val Pro 500 505 510 Pro Thr Pro Ala Pro Val Gly Ala Pro Leu Pro Ala Glu Ala Gly Gly 515 520 525 Gly Gln 530 13 1590 DNA Mycobacterium tuberculosis 13 ttgagcacca tctttgatat ccgcaacctg cggttgccgc agctgtcgcg ggcctcggtt 60 gtcatcggat cgttggtggt ggtgctggcg ctggccgccg gaattgttgg tgtgcggctc 120 tatcaaaaac tgacgaacaa cacggtggtc gcctacttca cccaagccaa tgcgctgtat 180 gtcggagaca aggtccagat tatgggcctc ccggtcggtt cgatcgacaa gatcgaacca 240 gccggcgaca aaatgaaggt gactttccac taccagaaca agtacaaggt gcctgccaat 300 gcctccgcgg tgatcctcaa ccccaccttg gtggcgtcgc ggaacattca gttggagcca 360 ccctacagag gtggtccagt gctggccgat aatgcggtga tcccggtcga gcgcacccag 420 gtaccgacgg agtgggacga gctgcgggac agcgtttcgc atattatcga cgagctcggc 480 ccgacacctg agcagcccaa ggggccgttc ggcgaagtca tcgaggcatt cgccgacggg 540 ctggccggca agggtaagca aatcaacacc acgctgaaca gcctgtcgca ggcgttgaac 600 gccttgaatg agggccgcgg cgacttcttc gcggtggtac gcagcctggc gctattcgtc 660 aacgcgctac atcaggacga ccaacagttc gtcgcgttga acaagaacct tgcggagttc 720 accgacaggt tgacccactc cgatgcggac ctgtcgaacg ccatccagca attcgacagc 780 ttgctcgccg tcgcgcgccc gttcttcgcc aagaaccgcg aggtgctgac gcatgacgtc 840 aataatctcg cgaccgtgac caccacgttg ctgcagcccg atccgttgga tgggttggag 900 accgtcctgc acatcttccc gacgctggcg gcgaacatta accagcttta ccatccgaca 960 cacggtggcg tggtgtcgct ttccgcgttc acgaatttcg ccaacccgat ggagttcatc 1020 tgcagctcga ttcaggcggg tagccggctc ggttatcaag agtcggccga actctgtgcg 1080 cagtatctgg cgccagtcct cgatgcgatc aagttcaact actttccgtt cggcctgaac 1140 gtggccagca ccgcctcgac actgcctaaa gagatcgcgt actccgagcc ccgcttgcag 1200 ccgcccaacg ggtacaagga caccacggtg cccggcatct gggtgccgga tacgccgttg 1260 tcacaccgca acacgcagcc cggttgggtg gtggcacccg ggatgcaagg ggttcaggtg 1320 ggaccgatca cgcagggttt gctgacgccg gagtccctgg ccgaactcat gggtggtccc 1380 gatatcgccc ctccgtcgtc agggctgcaa accccgcccg gacccccgaa tgcgtacgac 1440 gagtaccccg tgctgccgcc gatcggttta caggccccac aggtgccgat accaccgccg 1500 cctcctgggc ccgacgtaat cccgggtccg gtgccaccga cgccggcacc ggtgggggcg 1560 ccgttgcccg ctgaggcagg agggggtcaa 1590 14 390 PRT Mycobacterium tuberculosis 14 Met Met Ser Val Leu Ala Arg Met Arg Val Met Arg His Arg Ala Trp 1 5 10 15 Gln Gly Leu Val Leu Leu Val Leu Ala Leu Leu Leu Ser Ser Cys Gly 20 25 30 Trp Arg Gly Ile Ser Asn Val Ala Ile Pro Gly Gly Pro Gly Thr Gly 35 40 45 Pro Gly Ser Tyr Thr Ile Tyr Val Gln Met Pro Asp Thr Leu Ala Ile 50 55 60 Asn Gly Asn Ser Arg Val Met Val Ala Asp Val Trp Val Gly Ser Ile 65 70 75 80 Arg Ala Ile Lys Leu Lys Asn Trp Val Ala Thr Leu Thr Leu Ser Leu 85 90 95 Lys Lys Asp Val Thr Leu Pro Lys Asn Ala Thr Ala Lys Ile Gly Gln 100 105 110 Thr Ser Leu Leu Gly Ser Gln His Val Glu Leu Ala Ala Pro Pro Asp 115 120 125 Pro Ser Pro Val Pro Leu Lys Asp Gly Asp Thr Ile Pro Leu Lys Arg 130 135 140 Ser Ser Ala Tyr Pro Thr Thr Glu Gln Thr Leu Ala Ser Ile Ala Thr 145 150 155 160 Leu Leu Arg Gly Gly Gly Leu Val Asn Leu Glu Gly Ile Gln Gln Glu 165 170 175 Ile Asn Ala Ile Val Thr Gly Arg Ala Asp Gln Ile Arg Ala Phe Leu 180 185 190 Gly Lys Leu Asp Thr Phe Thr Asp Glu Leu Asn Gln Gln Arg Asp Asp 195 200 205 Ile Thr Arg Ala Ile Asp Ser Thr Asn Arg Leu Leu Ala Tyr Val Gly 210 215 220 Gly Arg Ser Glu Val Leu Asn Arg Val Leu Thr Asp Leu Pro Pro Leu 225 230 235 240 Ile Lys His Phe Ala Asp Lys Gln Glu Leu Leu Ile Asn Ala Ser Asp 245 250 255 Ala Val Gly Arg Leu Ser Gln Ser Ala Asp Gln Tyr Leu Ser Ala Ala 260 265 270 Arg Gly Asp Leu His Gln Asp Leu Gln Ala Leu Gln Cys Pro Leu Lys 275 280 285 Glu Leu Arg Arg Ala Ala Pro Tyr Leu Val Gly Ala Leu Lys Leu Ile 290 295 300 Leu Thr Gln Pro Phe Asp Val Asp Thr Val Pro Gln Leu Val Arg Gly 305 310 315 320 Asp Tyr Met Asn Leu Ser Leu Thr Leu Asp Leu Thr Tyr Ser Ala Ile 325 330 335 Asp Asn Ala Phe Leu Thr Gly Thr Gly Phe Ser Gly Ala Leu Arg Ala 340 345 350 Leu Glu Gln Ser Phe Gly Arg Asp Pro Glu Thr Met Ile Pro Asp Ile 355 360 365 Arg Tyr Thr Pro Asn Pro Asn Asp Ala Pro Gly Gly Pro Leu Val Glu 370 375 380 Arg Gly Asn Arg Gln Cys 385 390 15 1170 DNA Mycobacterium tuberculosis 15 atgatgagcg tgctggcgcg gatgcgggtg atgcgccacc gagcctggca ggggctggtg 60 ttgctggtgc tcgcactctt gctgagttcg tgcggctggc gcggcatctc caatgtggcg 120 atccccggcg gcccgggcac cggcccgggc tcctacacca tctacgtgca gatgccggac 180 acgttggcga tcaacggcaa cagtcgggtc atggtggccg acgtctgggt cggatcgatc 240 cgcgcgatca agttgaagaa ctgggtggcc acgctgacgc tgagcctgaa gaaggacgtc 300 acgctaccga aaaatgccac cgccaagatc gggcagacca gcctgctggg ttcgcagcac 360 gtcgagctgg ccgcgccgcc agatccgtcg ccggtgccgc tgaaggatgg tgacaccatc 420 ccgttgaagc gctcctcggc ctatcccacc accgagcaga cgctggccag catcgccacc 480 ttgttgcgcg gcggcggcct ggtgaacctc gaagggattc agcaagagat caacgccatc 540 gtgacggggc gggcggacca gatccgggcc tttcttggca agctcgacac cttcaccgac 600 gagctcaacc agcaacgcga tgacattacc cgcgccattg attccaccaa tcggttgttg 660 gcttatgtgg gcggtcgttc ggaagtcctc aatcgggtgc tcaccgacct accgccattg 720 atcaagcact ttgcggataa gcaggaactg ttgatcaacg cttccgatgc ggtaggccgg 780 ctcagccagt ccgccgacca gtatctttcg gctgcccggg gcgatctgca ccaggacctg 840 caggcgctgc aatgcccgct caaggaactg cgtcgagccg ctccgtatct ggtgggtgcg 900 ctcaaattga tcctcaccca gccctttgac gtcgacaccg tgccgcagct ggtgcggggc 960 gactacatga acttgtcgct gacgctggac ctgacctaca gcgccatcga caatgcgttc 1020 cttaccggga ccggattctc cggtgcgttg cgcgccctcg agcagtcttt tggccgcgat 1080 cccgagacaa tgattcccga catccggtac acaccgaacc ccaacgatgc gccgggcggc 1140 ccgctggtag aaaggggaaa tcgccagtgc 1170 16 515 PRT Mycobacterium tuberculosis 16 Val Leu Thr Arg Phe Ile Arg Arg Gln Leu Ile Leu Phe Ala Ile Val 1 5 10 15 Ser Val Val Ala Ile Val Val Leu Gly Trp Tyr Tyr Leu Arg Ile Pro 20 25 30 Ser Leu Val Gly Ile Gly Gln Tyr Thr Leu Lys Ala Asp Leu Pro Ala 35 40 45 Ser Gly Gly Leu Tyr Pro Thr Ala Asn Val Thr Tyr Arg Gly Ile Thr 50 55 60 Ile Gly Lys Val Thr Ala Val Glu Pro Thr Asp Gln Gly Ala Arg Val 65 70 75 80 Thr Met Ser Ile Ala Ser Asn Tyr Lys Ile Pro Val Asp Ala Ser Ala 85 90 95 Asn Val His Ser Val Ser Ala Val Gly Glu Gln Tyr Ile Asp Leu Val 100 105 110 Ser Thr Gly Ala Pro Gly Lys Tyr Phe Ser Ser Gly Gln Thr Ile Thr 115 120 125 Lys Gly Thr Val Pro Ser Glu Ile Gly Pro Ala Leu Asp Asn Ser Asn 130 135 140 Arg Gly Leu Ala Ala Leu Pro Thr Glu Lys Ile Gly Leu Leu Leu Asp 145 150 155 160 Glu Thr Ala Gln Ala Val Gly Gly Leu Gly Pro Ala Leu Gln Arg Leu 165 170 175 Val Asp Ser Thr Gln Ala Ile Val Gly Asp Phe Lys Thr Asn Ile Gly 180 185 190 Asp Val Asn Asp Ile Ile Glu Asn Ser Gly Pro Ile Leu Asp Ser Gln 195 200 205 Val Asn Thr Gly Asp Gln Ile Glu Arg Trp Ala Arg Lys Leu Asn Asn 210 215 220 Leu Ala Ala Gln Thr Ala Thr Arg Asp Gln Asn Val Arg Ser Ile Leu 225 230 235 240 Ser Gln Ala Ala Pro Thr Ala Asp Glu Val Asn Ala Val Phe Ser Gly 245 250 255 Val Arg Asp Ser Leu Pro Gln Thr Leu Ala Asn Leu Glu Val Val Phe 260 265 270 Asp Met Leu Lys Arg Tyr His Ala Gly Val Glu Gln Leu Leu Val Phe 275 280 285 Leu Pro Gln Gly Ala Ala Ile Ala Gln Thr Val Leu Thr Pro Thr Pro 290 295 300 Gly Ala Ala Gln Leu Pro Leu Ala Pro Ala Ile Asn Tyr Pro Pro Pro 305 310 315 320 Cys Leu Thr Gly Phe Leu Pro Ala Ser Glu Trp Arg Ser Pro Ala Asp 325 330 335 Thr Ser Pro Arg Pro Leu Pro Ser Gly Thr Tyr Cys Lys Ile Pro Gln 340 345 350 Asp Ala Gln Leu Gln Val Arg Gly Ala Arg Asn Ile Pro Cys Val Asp 355 360 365 Val Leu Gly Lys Arg Ala Ala Thr Pro Lys Glu Cys Arg Ser Lys Asp 370 375 380 Pro Tyr Val Pro Leu Gly Thr Asn Pro Trp Phe Gly Asp Pro Asn Gln 385 390 395 400 Ile Leu Thr Cys Pro Ala Pro Gly Ala Arg Cys Asp Gln Pro Val Lys 405 410 415 Pro Gly Leu Val Ile Pro Ala Pro Ser Ile Asn Thr Gly Leu Asn Pro 420 425 430 Ala Pro Ala Asp Gln Val Gln Gly Thr Pro Pro Pro Val Ser Asp Pro 435 440 445 Leu Gln Arg Pro Gly Ser Gly Thr Val Gln Cys Asn Gly Gln Gln Pro 450 455 460 Asn Pro Cys Val Tyr Thr Pro Thr Ser Gly Pro Ser Ala Val Tyr Ser 465 470 475 480 Pro Ala Ser Gly Glu Leu Val Gly Pro Asp Gly Val Lys Tyr Ala Val 485 490 495 Ala Asn Ser Ser Thr Thr Gly Asp Asp Gly Trp Lys Glu Met Leu Ala 500 505 510 Pro Ala Ser 515 17 1545 DNA Mycobacterium tuberculosis 17 gtgctgactc gcttcatccg acgccagttg atcctttttg cgatcgtctc cgtagtcgca 60 atcgtcgtat tgggctggta ctacctgcga attccgagtc tggtgggtat cgggcagtac 120 accttgaagg ccgacttgcc cgcatcgggt ggcctgtatc cgacggccaa tgtgacctac 180 cgcggtatca ccattggcaa ggttactgcc gtcgagccca ccgaccaggg cgcacgagtg 240 acgatgagca tcgccagcaa ctacaaaatc cccgtcgatg cctcggcgaa cgtgcattcg 300 gtgtcagcgg tgggcgagca gtacatcgac ctggtgtcca ccggtgctcc gggtaaatac 360 ttctcctccg gacagaccat caccaagggc accgttccca gtgagatcgg gccggcgctg 420 gacaattcca atcgcgggtt ggccgcattg cccacggaga agatcggctt gctgctcgac 480 gagaccgcgc aagcggtggg tgggctggga cccgcgttgc aacggttggt cgattccact 540 caagcgatcg tcggtgactt caaaaccaac attggcgacg tcaacgacat catcgagaac 600 tccgggccga ttttggacag ccaggtcaac acgggtgatc agatcgagcg ctgggcgcgc 660 aaattgaaca atctggccgc acagaccgcg accagggatc agaacgtgcg aagcatcctg 720 tcccaggcgg cccccaccgc cgatgaggtt aacgcggtat tcagcggtgt tcgcgattcg 780 ctgccacaga ccctggccaa tcttgaggtt gtgttcgata tgctcaagcg ctaccacgcc 840 ggcgtggagc aattgttggt gttcctccca cagggtgccg cgatcgcaca gaccgtactc 900 acgccaactc cgggtgctgc ccagctgccg ctcgcgccgg cgatcaacta tccgccgccg 960 tgcttgacgg gttttcttcc tgcatcggag tggcggtctc cggccgatac cagtcccagg 1020 ccgttgccgt cgggaaccta ttgcaagatt ccccaggatg cccagctgca agtccggggg 1080 gcgcgcaaca ttccctgtgt cgatgtcctg ggcaaacgag cggcgacgcc gaaggagtgc 1140 cgcagtaagg acccgtacgt tccgctgggt accaacccgt ggtttggtga tccgaaccag 1200 attctcacct gcccggcacc tggagcgcgc tgcgatcagc cggtgaagcc cgggttggtg 1260 attccggcgc cctcgatcaa caccggtttg aatccggcgc ccgccgatca ggtgcaagga 1320 acgcccccgc cggtcagtga cccgttgcaa agaccgggtt cgggtactgt gcagtgcaac 1380 gggcagcagc ctaacccgtg cgtctacact ccaacatcgg gcccgtcggc ggtctatagc 1440 ccggccagcg gtgaactggt ggggccggat ggtgtcaagt acgccgtcgc aaactcgagc 1500 acaacaggag acgacggatg gaaggagatg ctggcgccgg ccagc 1545 18 1420 DNA Mycobacterium tuberculosis 18 gatctcggca ctacacaggt ccccgtggga gatctgctgg tcgtgcaggg tccgtagcgc 60 ctcccagaca tgggcagtcg gcgtggtttt ggtgcattcg ctgatgccga ttccgcgagc 120 gggccggtgt gcatacaacg tccatccccg gtcgagcggg gacaccgcga tcaccgtcgt 180 gttggccatg cctagatcgc cgaaggcaat ggccatcagc gcgcgatgct cgaccgcacg 240 gcgcatggag gcttgcaggg gtgcggtctc ggtgccgcgc aacgtcagct tcagccagag 300 ttggcgcagc gcgccgccgc cactttggtg cgggccgtac aactcgatca atgcctcgct 360 gcacgccccg gcgttgggct gctcgcaagc ggccgacagt accagtggcc cgggcccggc 420 cggccgcaca accgcgagcc cggacaccgc gaatccgcgt tttgccaacg cgcgaatggc 480 accatccagt ggcacttcaa gcgctggtgt gccgacgacc aggaccacca acgcgccgac 540 caaccacccc accgccagcc ccaacaatga gcgggccggc acaatcgcgc tgacaaccag 600 atggatcggc acgaatgcca acagcagcgc ccaccaccag tgccgccagc gcgcgggcag 660 ccagggaccc gacacggtga gcaccgccgc gagcatcgcg atccatcgcg ggtcatcgag 720 aaactgggcc agcaatgtgg cgagccggtc ggaaaggtca aagtgccatc ggggtgccgc 780 gatgcggcta ctgctgatcg acaacgggag aacggccata agtccggcgg ccgcatacgc 840 gcccagcagc ttccactgcc gggaaacgat caggccaatc aggatcacga acggcaacgc 900 caaaatcgcc aggccgtacc ccaggtacac cagatcggat tgcgacgggg acagcacccc 960 gacgatctcc gagatggatt tctccagcgc cacccactgc gggcgggtga tcagcgaact 1020 cgtgatcacc gccacgaggt agatcgccgc cagcaccgcc cggatgatgt cgttggtgcg 1080 ccgggtcagt ggttgcagca agttaccgga aacgccgatg tcgcgtccgt caactcgcat 1140 gttctaacga tcttccgaat cagggcccgc ggtgtctggt gccgtttcgc ggctccgcgg 1200 acaacttagc ccgataactg cgtggggtgt cggtctgacc acttgacgtc ttaccaatct 1260 tcattcacac tgggcgcatg gcgctgcagc cggtgactcg ccgatcggtg cccgaagagg 1320 tcttcgagca gatcgctacc gatgtgctca ccggcgagat gccgcccggc gaggcgttgc 1380 ccagcgagcg tcggttggct gagttgctcg gagtgtcgcg 1420 19 240 PRT Mycobacterium tuberculosis 19 Met Ala Leu Gln Pro Val Thr Arg Arg Ser Val Pro Glu Glu Val Phe 1 5 10 15 Glu Gln Ile Ala Thr Asp Val Leu Thr Gly Glu Met Pro Pro Gly Glu 20 25 30 Ala Leu Pro Ser Glu Arg Arg Leu Ala Glu Leu Leu Gly Val Ser Arg 35 40 45 Pro Ala Val Arg Glu Ala Leu Lys Arg Leu Ser Ala Ala Gly Leu Val 50 55 60 Glu Val Arg Gln Gly Asp Val Thr Thr Val Arg Asp Phe Arg Arg His 65 70 75 80 Ala Gly Leu Asp Leu Leu Pro Arg Leu Leu Phe Arg Asn Gly Glu Leu 85 90 95 Asp Ile Ser Val Val Arg Ser Ile Leu Glu Ala Arg Leu Arg Asn Phe 100 105 110 Pro Lys Val Ala Glu Leu Ala Ala Glu Arg Asn Glu Pro Glu Leu Ala 115 120 125 Glu Leu Leu Gln Asp Ser Leu Arg Ala Leu Asp Thr Glu Glu Asp Pro 130 135 140 Ile Val Trp Gln Arg His Thr Leu Asp Phe Trp Asp His Val Val Asp 145 150 155 160 Ser Ala Gly Ser Ile Val Asp Arg Leu Met Tyr Asn Ala Phe Arg Ala 165 170 175 Ala Tyr Glu Pro Thr Leu Ala Ala Leu Thr Thr Thr Met Thr Ala Ala 180 185 190 Ala Lys Arg Pro Ser Asp Tyr Arg Lys Leu Ala Asp Ala Ile Cys Ser 195 200 205 Gly Asp Pro Thr Gly Ala Lys Lys Ala Ala Gln Asp Leu Leu Glu Leu 210 215 220 Ala Asn Thr Ser Leu Met Ala Val Leu Val Ser Gln Ala Ser Arg Gln 225 230 235 240 20 720 DNA Mycobacterium tuberculosis 20 atggcgctgc agccggtgac tcgccgatcg gtgcccgaag aggtcttcga gcagatcgct 60 accgatgtgc tcaccggcga gatgccgccc ggcgaggcgt tgcccagcga gcgtcggttg 120 gctgagttgc tcggagtgtc gcgacccgcg gtccgcgagg cgctcaaacg gctgtcggcc 180 gcaggtctgg tcgaggtgcg tcagggcgac gtcaccaccg tgcgtgactt ccggcggcac 240 gccggcctgg atctgttgcc ccgattgttg tttcgcaacg gtgagctgga tatctccgtc 300 gtccgcagca tcctcgaggc ccggctgcgc aattttccga aggtcgcgga actagcggcc 360 gaacggaacg agcccgagtt ggcggaattg ctgcaggatt cgctgcgtgc gctggacact 420 gaggaagatc cgatcgtgtg gcaacgccac acgctcgact tttgggatca tgtggtcgac 480 agcgccggtt cgatcgtaga tcgattgatg tacaacgcat ttcgtgctgc ttacgagccg 540 acgctagctg ctctgaccac cacgatgacc gctgcggcta agcgtccgtc ggactaccgg 600 aaactcgcgg atgcgatctg ctcaggtgat cccaccggag cgaagaaagc cgcccaagac 660 ctactcgaac ttgcgaacac atcgttgatg gccgtactcg ttagccaggc gagtcggcaa 720 21 265 PRT Mycobacterium tuberculosis 21 Met Thr Thr His Ala Val Ile Ile Thr Tyr Leu Arg Asp Gln Thr Gln 1 5 10 15 Pro Ala Val Asp Ala Ile Gly Gly Phe Tyr Arg Thr Cys Val Leu Thr 20 25 30 Gly Lys Ala Leu Val Arg Arg Pro Phe His Trp Arg Glu Ala Ile Glu 35 40 45 Gln Gly Trp Phe Ile Thr Ser Val Ser Leu Leu Pro Thr Leu Ala Val 50 55 60 Ser Ile Pro Leu Thr Val Leu Ile Ile Phe Thr Leu Asn Ile Leu Leu 65 70 75 80 Ala Glu Phe Gly Ala Ala Asp Ile Ser Gly Ala Gly Ala Ala Leu Gly 85 90 95 Ala Val Thr Gln Leu Gly Pro Leu Thr Thr Val Leu Val Ile Ala Gly 100 105 110 Ala Gly Ala Thr Ala Ile Cys Ala Asp Leu Gly Ala Arg Thr Ile Arg 115 120 125 Glu Glu Ile Asp Ala Met Glu Val Leu Gly Ile Asp Pro Ile His Arg 130 135 140 Leu Val Val Pro Arg Val Val Ala Ala Thr Ile Val Ala Ala Leu Leu 145 150 155 160 Asn Gly Ala Val Ile Thr Ile Gly Leu Val Gly Gly Phe Val Phe Ser 165 170 175 Val Phe Ile Gln His Val Ser Ala Gly Ala Tyr Val Gly Thr Leu Thr 180 185 190 Leu Val Thr Gly Leu Pro Glu Val Ile Ile Ser Val Val Lys Ser Ala 195 200 205 Thr Phe Gly Leu Ile Ala Gly Leu Val Gly Cys Tyr Arg Gly Leu Thr 210 215 220 Thr Lys Gly Gly Pro Lys Gly Val Gly Thr Ala Val Asn Glu Thr Leu 225 230 235 240 Val Leu Cys Val Ile Ala Leu Phe Ala Thr Asn Val Val Leu Thr Thr 245 250 255 Ile Gly Val Arg Phe Gly Thr Gly His 260 265 22 795 DNA Mycobacterium tuberculosis 22 atgaccaccc acgccgtgat catcacctat ctccgcgacc agacgcagcc cgccgtcgat 60 gcgatcggcg ggttctaccg gacatgcgta ctgactggca aggcgctggt tcggcggccc 120 ttccattggc gtgaggcgat cgagcagggc tggttcatta ccagcgtctc gttgctgcca 180 accctggcgg tgtcgattcc gttgaccgtg ttgatcatct tcacgctcaa tatcctgctg 240 gccgagttcg gcgccgccga catctccggc gccggcgcgg cgctaggcgc ggtcacccag 300 ctgggcccgc tgaccaccgt gttggtgatt gccggcgctg gagccacagc gatctgcgcc 360 gacctgggtg cccgcaccat ccgggaagag atcgatgcga tggaggtgct gggcatcgac 420 cccatccacc ggctggtggt gcctcgggtc gttgccgcga ccatcgtcgc cgcactgctt 480 aacggcgcgg tgataaccat tggcctggtt ggtggtttcg tcttcagtgt cttcatccaa 540 cacgtctcgg ccggcgccta cgtgggcacg ctcaccttgg tcaccggtct acccgaggtg 600 atcatctcgg tggtcaagtc ggcgacgttc ggcctgatcg ctggcctagt cggctgttac 660 cgcgggctga ccacgaaagg cggccccaag ggagttggaa ccgccgtcaa cgaaaccctg 720 gtgctgtgcg tgatcgcgct gttcgcgacc aatgtggtgt tgaccacgat cggcgtgcgg 780 ttcgggacgg gacac 795 23 295 PRT Mycobacterium tuberculosis 23 Met Val Glu Ser Ser Thr Ala Ser Ala Ala Ala Val Leu Arg Ala Arg 1 5 10 15 Tyr Pro Arg Thr Ala Ala Ser Leu Asp Arg Tyr Gly Gly Gly Thr Ala 20 25 30 Arg Arg Leu Glu Arg Thr Gly Thr Phe Ala Arg Phe Thr Arg Ile Ser 35 40 45 Val Val Gln Ile Gly Trp Ala Leu Arg Arg Tyr Arg Arg Glu Thr Leu 50 55 60 Arg Leu Val Ala Glu Ile Gly Met Gly Thr Gly Ala Met Ala Val Val 65 70 75 80 Gly Gly Thr Val Ala Ile Ile Gly Phe Val Thr Leu Ser Gly Gly Ser 85 90 95 Leu Ile Ala Ile Gln Gly Phe Ala Ser Leu Gly Asn Ile Gly Val Glu 100 105 110 Ala Phe Thr Gly Phe Phe Ala Ala Leu Ala Asn Thr Arg Val Ala Ala 115 120 125 Pro Ile Val Ser Gly Val Ala Leu Ala Ala Thr Val Gly Ala Gly Ala 130 135 140 Thr Ala Gln Leu Gly Ala Met Arg Ile Ser Glu Glu Ile Asp Ala Leu 145 150 155 160 Glu Val Met Gly Ile Lys Ser Ile Ser Phe Leu Val Ser Thr Arg Ile 165 170 175 Leu Gly Gly Leu Val Val Ile Met Pro Leu Tyr Ala Leu Ala Leu Asp 180 185 190 Met Ala Phe Thr Ser Gly Gln Val Val Thr Thr Val Phe Tyr Gly Gln 195 200 205 Ser Asn Gly Thr Tyr Glu His Tyr Phe Arg Thr Phe Leu Arg Pro Glu 210 215 220 Asp Val Gly Trp Ser Val Val Glu Val Val Ile Ile Ala Val Val Val 225 230 235 240 Met Ile Thr His Cys Tyr Tyr Gly Tyr Thr Ala Ser Gly Gly Pro Val 245 250 255 Gly Val Gly Gln Ala Val Gly Arg Ser Met Arg Phe Ser Leu Val Ser 260 265 270 Val Val Val Val Val Leu Leu Ala Glu Leu Ala Leu Tyr Gly Val Asp 275 280 285 Pro Asn Phe Asn Leu Thr Val 290 295 24 885 DNA Mycobacterium tuberculosis 24 atggtggagt cttcaacggc atcagcggca gccgtattgc gggcccgcta cccacgcaca 60 gccgccagcc ttgaccgcta cggcggcggc acggcccgaa gacttgagcg gacagggact 120 ttcgcgagat tcacccggat cagcgtcgtg cagatcggct gggcactgcg tcgctatcgc 180 cgggagacgc tgcgcctggt cgccgagatc gggatgggca ccggcgcgat ggccgtcgtc 240 ggcggcacgg tcgcgatcat cggttttgtg acgctgtccg gcggctcgct gatcgccatc 300 cagggcttcg cgtcgctggg caacatcggt gtcgaggcgt ttaccggatt ctttgccgca 360 ctggccaaca cacgcgtcgc tgcgcccatt gtctccggtg tcgcgctggc cgcgacggtg 420 ggcgccggcg ccaccgcaca gttaggtgcc atgcggatca gtgaggagat cgacgcgctg 480 gaagtgatgg gcatcaagtc gatttcgttt ctggtctcca ctcggattct aggagggctg 540 gtggtgatca tgccgctgta cgcgctcgct ctcgacatgg ctttcacctc tggtcaggtg 600 gtcacaaccg tgttctacgg ccagtccaac ggcacctatg agcactactt ccgcaccttc 660 ctgcgcccag aggatgtggg ttggtcggtc gtggaggtgg tgatcatcgc ggtggtggtg 720 atgatcaccc attgctacta cgggtacacc gccagcggtg gcccggttgg ggtcggccag 780 gcggttggtc gatcgatgcg tttctcgctg gtctcggtgg tggtcgttgt cctgctggcc 840 gagttggcgc tctacggcgt cgacccgaac ttcaatctca cggtg 885 25 404 PRT Mycobacterium tuberculosis 25 Val Pro Thr Leu Val Thr Arg Lys Asn Arg Arg Ala Trp Leu Tyr Val 1 5 10 15 Glu Gly Val Val Leu Leu Leu Val Gly Ala Leu Val Leu Val Leu Val 20 25 30 Tyr Lys Gln Phe Arg Gly Glu Phe Thr Pro Lys Thr Glu Leu Thr Met 35 40 45 Val Ala Phe Arg Ala Gly Leu Val Met Glu Ala Gly Ser Lys Val Thr 50 55 60 Tyr Asn Gly Val Glu Ile Gly Arg Val Gly Ser Ile Ser Glu Ile Glu 65 70 75 80 Arg Asp Gly Arg Pro Ala Ala Lys Leu Val Leu Asp Val Asn Pro Arg 85 90 95 Tyr Ile Ser Leu Ile Pro Val Asn Val Val Ala Asp Ile Glu Ala Ala 100 105 110 Thr Leu Phe Gly Asn Lys Tyr Val Ala Leu Ser Ala Pro Lys Ile Pro 115 120 125 Gln Gln Gln Arg Ile Ser Ser His Asp Val Ile Asp Val Gly Ser Val 130 135 140 Thr Thr Glu Phe Asn Thr Leu Phe Glu Thr Ile Thr Ser Ile Ala Glu 145 150 155 160 Lys Val Asp Pro Ile Glu Leu Asn Ala Thr Leu Ser Ala Val Ala Gln 165 170 175 Ala Leu Asp Gly Leu Gly Gly Lys Phe Gly Glu Ser Ile Val Asn Gly 180 185 190 Asn Gln Ile Leu Ala Gln Leu Asn Pro Arg Leu Pro Gln Leu Gly Tyr 195 200 205 Asp Val Arg Arg Leu Ala Asp Leu Gly Glu Val Tyr Val Asp Ala Ser 210 215 220 Pro Asp Leu Trp Ser Phe Leu Gln Asn Ala Leu Thr Thr Ala Arg Thr 225 230 235 240 Leu Thr Ser Gln Gln Arg Asp Leu Asp Ala Ala Leu Leu Ala Ala Thr 245 250 255 Gly Ala Gly Asn Thr Gly Glu Asp Val Phe Ala Arg Gly Gly Pro Tyr 260 265 270 Leu Ala Arg Ala Ala Ala Asp Leu Val Pro Thr Ala Thr Leu Leu Asp 275 280 285 Thr Tyr Ser Pro Glu Leu Phe Cys Met Ile Arg Asn Phe His Asp Ala 290 295 300 Ala Pro Lys Val Ala Asp Ala Val Gly Gly Asn Gly Tyr Ser Leu Ala 305 310 315 320 Ala Ala Gly Thr Ile Leu Gly Ala Pro Asn Pro Tyr Val Tyr Pro Asp 325 330 335 Asn Leu Pro Arg Val Asn Ala His Gly Gly Pro Gly Gly Arg Pro Gly 340 345 350 Cys Trp Gln Thr Ile Thr Arg Glu Leu Trp Pro Ala Pro Tyr Leu Val 355 360 365 Met Asp Thr Gly Ala Ser Leu Ala Pro Tyr Asn His Val Glu Leu Gly 370 375 380 Gln Pro Met Phe Thr Glu Tyr Val Trp Gly Arg Gln Tyr Gly Glu Asn 385 390 395 400 Thr Ile Asn Pro 26 1212 DNA Mycobacterium tuberculosis 26 gtgccaacgc tggtgacgag gaagaaccga cgtgcgtggc tgtatgtgga gggtgttgtc 60 ctgctgttgg tgggcgcgtt ggtgctcgta ttggtgtaca agcagtttcg tggggaattc 120 acgccgaaga ccgagctgac tatggtcgcc ttccgggctg ggctggttat ggaagctgga 180 tccaaagtca cctacaacgg ggtggagatc ggccgggtgg gcagcatttc ggagattgag 240 cgtgacggcc ggccggcggc gaagctggtt ttggacgtga atcctcgcta catcagcctg 300 attccggtca atgtggtggc cgatatcgag gcggccaccc tgttcggcaa caagtatgtt 360 gcgctgtccg cgccgaaaat tcctcaacag cagcggattt cctcacatga cgtgattgat 420 gtggggtcgg tgaccaccga attcaacacg ttgttcgaga cgatcacctc gatcgccgag 480 aaggtggatc cgatcgagct gaacgcgacg ctgtccgcgg tagcacaggc gctggatggg 540 ctgggcggca agttcggtga gtcgatcgtt aatggcaatc agattctggc gcaattaaat 600 ccgcggctgc cgcagctcgg ctatgatgtt cggcggttgg cggatctcgg tgaggtctat 660 gtcgatgctt cgccggatct gtggtccttt ctgcagaacg cactgaccac tgcgcgcaca 720 ttgaccagcc aacagcgcga tctggatgcc gcgttgttgg cggctacggg tgcgggcaac 780 accggtgaag acgtttttgc tcgaggcggg ccgtatcttg cgcgcgcagc cgccgatctg 840 gtgcccaccg ctacgctgct ggacacctac agtcccgaac tgttctgcat gatccgcaac 900 tttcacgacg ctgcgcccaa agtcgcggac gcggtgggcg gcaacggcta ttcgctagcg 960 gccgccggaa cgattttggg agcacccaat ccctatgtct atccggacaa tctgccgcgg 1020 gtgaatgccc acggtggacc cgggggccga ccgggctgct ggcagacgat cacccgggag 1080 ctgtggccgg caccctatct ggtgatggac accggtgcca gcctcgcacc gtacaaccac 1140 gtcgagctcg gccaaccgat gttcactgaa tacgtatggg gacgccaata cggagagaac 1200 acgatcaacc ca 1212 27 275 PRT Mycobacterium tuberculosis 27 Met Lys Thr Thr Gly Thr Thr Ile Lys Leu Gly Ile Val Trp Leu Val 1 5 10 15 Leu Ser Val Phe Thr Val Met Ile Ile Val Val Phe Gly Gln Val Arg 20 25 30 Phe His His Thr Thr Gly Tyr Ser Ala Val Phe Thr His Val Ser Gly 35 40 45 Leu Arg Ala Gly Gln Phe Val Arg Ala Ala Gly Val Glu Val Gly Lys 50 55 60 Val Ala Lys Val Thr Leu Ile Asp Gly Asp Lys Gln Val Leu Val Asp 65 70 75 80 Phe Thr Val Asp Arg Ser Leu Ser Leu Asp Gln Ala Thr Thr Ala Ser 85 90 95 Ile Arg Tyr Leu Asn Leu Ile Gly Asp Arg Tyr Leu Glu Leu Gly Arg 100 105 110 Gly His Ser Gly Gln Arg Leu Ala Pro Gly Ala Thr Ile Pro Leu Glu 115 120 125 His Thr His Pro Ala Leu Asp Leu Asp Ala Leu Leu Gly Gly Phe Arg 130 135 140 Pro Leu Phe Gln Thr Leu Asp Pro Asp Lys Val Asn Ser Ile Ala Ser 145 150 155 160 Ser Ile Ile Thr Val Phe Gln Gly Gln Gly Ala Thr Ile Asn Asp Ile 165 170 175 Leu Asp Gln Thr Ala Ser Leu Thr Ala Thr Leu Ala Asp Arg Asp His 180 185 190 Ala Ile Gly Glu Val Val Asn Asn Leu Asn Thr Val Leu Ala Thr Thr 195 200 205 Val Lys His Gln Thr Glu Phe Asp Arg Thr Val Asp Lys Leu Glu Val 210 215 220 Leu Ile Thr Gly Leu Lys Asn Arg Ala Asp Pro Leu Ala Ala Ala Ala 225 230 235 240 Ala His Ile Ser Ser Ala Ala Gly Thr Leu Ala Asp Leu Leu Gly Arg 245 250 255 Ile Val His Cys Cys Thr Ala Ala Ser Gly Thr Ser Arg Ala Ser Ser 260 265 270 Ser Arg Ser 275 28 825 DNA Mycobacterium tuberculosis 28 atgaaaacca caggcacaac tatcaaactc ggcatcgtct ggttggtgct gtcggtgttc 60 accgtgatga tcatcgtggt gttcgggcag gtgcggttcc atcacaccac cgggtactcc 120 gcggtgttca cccatgtcag cgggctgcgg gccgggcaat ttgtccgcgc tgcgggcgta 180 gaggtcggca aggtcgccaa ggtaacgctg atcgacgggg acaagcaagt attggtggac 240 ttcaccgtgg atcgctcgct gtcactggat caggcgacga ccgcctcgat ccgctacctc 300 aacctgatcg gcgaccggta ccttgagctc ggccgcggtc acagcggtca gcggctggcg 360 ccgggtgcca cgatcccgct cgagcacacc catccggcct tggatctcga cgctctgctc 420 ggcgggtttc gcccactctt ccaaacgttg gacccagaca aggtcaacag catcgcctcc 480 tcgatcatca ccgtgttcca agggcaaggc gccaccatca acgacatcct cgaccagacc 540 gcctcgctga cggcaacgct ggccgaccgg gaccatgcga taggtgaggt cgtcaacaac 600 ttgaacaccg tgctggccac caccgtcaag catcaaacgg aattcgaccg cacggtcgac 660 aagctagagg tgctgatcac tggactgaag aacagggcgg acccgctggc cgcggcggcg 720 gcacacatca gcagcgccgc gggaacccta gccgacctgc tggggcggat cgtccattgc 780 tgcacagcag cttcgggcac ctcgagggca tccagcagcc gctca 825 29 481 PRT Mycobacterium tuberculosis 29 Met Arg Thr Leu Thr Glu Phe Asn Arg Gly Arg Val Gly Met Met Gly 1 5 10 15 Ala Val Val Thr Val Leu Val Val Gly Val Ala Gln Ser Phe Thr Ser 20 25 30 Val Pro Met Leu Phe Ala Thr Pro Thr Tyr Tyr Ala Gln Phe Ala Asp 35 40 45 Thr Gly Gly Ile Asn Thr Gly Asp Lys Val Glu Ile Ala Gly Val Asn 50 55 60 Val Gly Leu Val Arg Ser Leu Ala Ile Arg Gly Asn Arg Val Leu Ile 65 70 75 80 Gly Phe Ser Leu Pro Gly Lys Thr Ile Gly Met Gln Ser Arg Ala Ala 85 90 95 Ile Arg Thr Asp Thr Ile Leu Gly Arg Lys Asn Leu Glu Ile Glu Pro 100 105 110 Arg Gly Ser Glu Pro Leu Lys Pro Asn Gly Phe Leu Pro Leu Ala Gln 115 120 125 Thr Thr Thr Pro Tyr Gln Ile Tyr Asp Ala Phe Val Asp Val Thr Lys 130 135 140 Ala Ala Thr Gly Trp Asp Ile Asp Ala Val Lys Arg Ser Leu Asn Val 145 150 155 160 Leu Ser Glu Thr Phe Asp Gln Thr Ala Pro His Leu Ser Ala Ala Leu 165 170 175 Glu Gly Val Lys Ala Phe Ser Asp Thr Val Gly Arg Arg Gly Glu Gln 180 185 190 Ile Glu Gln Leu Leu Ala Asn Ala Asn Arg Ile Ala Arg Val Leu Gly 195 200 205 Asp Arg Ser Glu Gln Val Asn Gly Leu Leu Val Asn Ala Lys Thr Leu 210 215 220 Leu Ala Ala Phe Lys Gln Arg Ser Gln Ala Leu Arg Ile Leu Leu Thr 225 230 235 240 Asn Val Ser Glu Ala Ser Ala Gln Val Ser Gly Leu Ile Thr Asp Asn 245 250 255 Pro Asn Leu Asn His Val Leu Ala Gln Leu Arg Thr Val Ser Glu Glu 260 265 270 Leu Val Lys Arg Lys Asn Glu Leu Ala Asp Val Ala Val Leu Leu Gly 275 280 285 Arg Tyr Thr Ala Ala Leu Thr Glu Ala Val Gly Ser Gly Pro Phe Phe 290 295 300 Lys Ala Met Val Val Asn Leu Leu Pro Tyr Gln Ile Leu Gln Pro Trp 305 310 315 320 Val Asp Ala Ala Phe Lys Lys Arg Gly Ile Asp Pro Glu Asn Phe Trp 325 330 335 Arg Ser Ala Gly Leu Pro Glu Phe Arg Trp Pro Asp Pro Asn Gly Thr 340 345 350 Arg Phe Pro Asn Gly Ala Pro Pro Ala Ala Pro Pro Val Arg Glu Gly 355 360 365 Thr Pro Lys His Pro Gly Pro Ala Val Pro Pro Gly Thr Pro Cys Ser 370 375 380 Tyr Thr Pro Ala Ala Gly Ala Leu Pro Arg Pro Asp Thr Pro Leu Pro 385 390 395 400 Cys Ala Gly Ala Thr Val Gly Pro Phe Gly Gly Pro Asp Phe Pro Ala 405 410 415 Pro Leu Asp Val Gln Pro Ser Pro Pro Asn Pro Asp Gly Pro Pro Pro 420 425 430 Thr Pro Gly Ile Leu Ser Ala Gly Arg Pro Gly Glu Pro Ala Pro Ala 435 440 445 Val Pro Gly Ile Pro Met Pro Leu Pro Pro Asn Ala Pro Pro Gly Ala 450 455 460 Arg Thr Gln Pro Leu Glu Pro Phe Pro Asp Gly Thr Gly Gly Ser Asn 465 470 475 480 Gln 30 1443 DNA Mycobacterium tuberculosis 30 atgagaacgc tgaccgagtt caaccgcggc cgtgtcggga tgatgggtgc ggtggtcacg 60 gtgctcgtcg ttggtgttgc gcaaagcttc accagcgtgc cgatgctgtt cgccacacct 120 acctactatg cgcaattcgc cgacacgggt ggcatcaaca cgggcgataa ggtggaaatc 180 gctggggtga acgtcgggct ggtgcgctcg ctggcaatcc gcggcaaccg cgtgttgatc 240 ggattctcgt tgcccggcaa gacaatcggg atgcaaagcc gggcagcaat tcgcaccgac 300 accattcttg gccgtaagaa cctggagatc gaaccccgcg gttcggagcc gttgaaaccc 360 aacggtttcc tgccgttggc gcagaccact acgccatacc aaatctatga cgcgttcgtc 420 gatgtcacga aggcggcgac gggctgggac atcgatgccg tcaaacgctc gctaaacgtg 480 ttgtcggaga cattcgatca gaccgccccg catctaagtg ccgccctcga gggtgtcaag 540 gcattctccg acaccgtcgg ccggcgcggc gagcagatcg agcaactgct ggcgaacgcc 600 aacaggatcg cgcgcgtgct cggcgaccgc agcgagcagg tcaacgggct gctggtgaat 660 gccaagacgc tgctggccgc gttcaagcaa cgcagccagg cactgcgcat tctgctaacc 720 aacgtgtcgg aggcatcagc ccaggtatct ggcctgatca cagacaaccc caacctcaac 780 catgtgctgg cccagttgcg cacggtcagc gaggagctgg tgaagcgcaa gaacgaattg 840 gccgatgtag ccgtcttgct cggcagatac accgcggccc tgacagaggc cgtcggttcc 900 ggaccgttct tcaaggcgat ggtggtcaat ctgctgccct accagattct tcagccctgg 960 gttgacgcgg cgttcaaaaa gcggggcatc gacccggaga acttctggcg cagtgcgggt 1020 ctgccggaat tccgctggcc cgaccccaac ggcacccggt tccccaacgg cgcgccgccg 1080 gcggcgccac cggtgcggga gggtacaccc aagcatccgg gaccggccgt cccgccggga 1140 acgccgtgct cctacacacc ggcggcgggc gcgttgccac ggcccgacac cccactaccc 1200 tgcgcgggcg ccaccgttgg cccgttcggt ggacccgact tcccggcacc gctcgatgtc 1260 cagccgtcgc cgcctaatcc cgatgggccg ccgccgacgc cgggcatcct aagtgctggg 1320 cggccgggcg agccggctcc ggctgttccg ggcataccga tgccgctgcc gccgaacgcg 1380 ccgccgggtg cacgcaccca accgcttgag ccgtttcctg acgggacggg aggtagcaac 1440 caa 1443 31 508 PRT Mycobacterium tuberculosis 31 Met Ser Thr Ile Phe Asp Ile Arg Ser Leu Arg Leu Pro Lys Leu Ser 1 5 10 15 Ala Lys Val Val Val Val Gly Gly Leu Val Val Val Leu Ala Val Val 20 25 30 Ala Ala Ala Ala Gly Ala Arg Leu Tyr Arg Lys Leu Thr Thr Thr Thr 35 40 45 Val Val Ala Tyr Phe Ser Glu Ala Leu Ala Leu Tyr Pro Gly Asp Lys 50 55 60 Val Gln Ile Met Gly Val Arg Val Gly Ser Ile Asp Lys Ile Glu Pro 65 70 75 80 Ala Gly Asp Lys Met Arg Val Thr Leu His Tyr Ser Asn Lys Tyr Gln 85 90 95 Val Pro Ala Thr Ala Thr Ala Ser Ile Leu Asn Pro Ser Leu Val Ala 100 105 110 Ser Arg Thr Ile Gln Leu Ser Pro Pro Tyr Thr Gly Gly Pro Val Leu 115 120 125 Gln Asp Gly Ala Val Ile Pro Ile Glu Arg Thr Gln Val Pro Val Glu 130 135 140 Trp Asp Gln Leu Arg Asp Ser Ile Asn Gly Ile Leu Arg Gln Leu Gly 145 150 155 160 Pro Thr Glu Arg Gln Pro Lys Gly Pro Phe Gly Asp Leu Ile Glu Ser 165 170 175 Ala Ala Asp Asn Leu Ala Gly Lys Gly Arg Gln Leu Asn Glu Thr Leu 180 185 190 Asn Ser Leu Ser Gln Ala Leu Thr Ala Leu Asn Glu Gly Arg Gly Asp 195 200 205 Phe Val Ala Ile Thr Arg Ser Leu Ala Leu Phe Val Ser Ala Leu Tyr 210 215 220 Gln Asn Asp Gln Gln Phe Val Ala Leu Asn Glu Asn Leu Ala Glu Phe 225 230 235 240 Thr Asp Trp Phe Thr Lys Ser Asp His Asp Leu Ala Asp Thr Val Glu 245 250 255 Arg Ile Asp Asp Val Leu Gly Thr Val Arg Lys Phe Val Ser Asp Asn 260 265 270 Arg Ser Val Leu Ala Ala Asp Val Asn Asn Leu Ala Asp Ala Thr Thr 275 280 285 Thr Leu Val Gln Pro Glu Pro Arg Asp Gly Leu Glu Thr Ala Leu His 290 295 300 Val Leu Pro Thr Tyr Ala Ser Asn Phe Asn Asn Leu Tyr Tyr Pro Leu 305 310 315 320 His Ser Ser Leu Val Gly Gln Phe Val Phe Pro Asn Phe Ala Asn Pro 325 330 335 Ile Gln Leu Ile Cys Ser Ala Ile Gln Ala Gly Ser Arg Leu Gly Tyr 340 345 350 Gln Glu Ser Ala Glu Leu Cys Ala Gln Tyr Leu Ala Pro Val Leu Asp 355 360 365 Ala Leu Lys Phe Asn Tyr Leu Pro Phe Gly Ser Asn Pro Phe Ser Ser 370 375 380 Ala Ala Thr Leu Pro Lys Glu Val Ala Tyr Ser Glu Glu Arg Leu Arg 385 390 395 400 Pro Pro Pro Gly Tyr Lys Asp Thr Thr Val Pro Gly Ile Phe Ser Arg 405 410 415 Asp Thr Pro Phe Ser His Gly Asn His Glu Pro Gly Trp Val Val Ala 420 425 430 Pro Gly Met Gln Gly Met Gln Val Gln Pro Phe Thr Ala Asn Met Leu 435 440 445 Thr Pro Glu Ser Leu Ala Glu Leu Leu Gly Gly Pro Asp Ile Ala Pro 450 455 460 Pro Pro Pro Gly Thr Asn Leu Pro Gly Pro Pro Asn Ala Tyr Asp Glu 465 470 475 480 Ser Asn Pro Leu Pro Pro Pro Trp Tyr Pro Gln Pro Ala Ser Leu Pro 485 490 495 Ala Ala Gly Ala Thr Gly Gln Pro Gly Pro Gly Gln 500 505 32 1524 DNA Mycobacterium tuberculosis 32 atgagcacca tcttcgacat ccgcagcctg cgactgccga aactgtctgc aaaggtagtg 60 gtcgtcggcg ggttggtggt ggtcttggcg gtcgtggccg ctgcggccgg cgcgcggctc 120 taccggaaac tgactaccac taccgtggtc gcgtatttct ctgaggcgct cgcgctgtac 180 ccaggagaca aagtccagat catgggtgtg cgggtcggtt ctatcgacaa gatcgagccg 240 gccggcgaca agatgcgagt cacgttgcac tacagcaaca aataccaggt gccggccacg 300 gctaccgcgt cgatcctcaa ccccagcctg gtggcctcgc gcaccatcca gctgtcaccg 360 ccgtacaccg gcggcccggt cttgcaagac ggcgcggtga tcccaatcga gcgcacccag 420 gtgcccgtcg agtgggatca gttgcgcgat tccatcaatg ggatcctccg ccagctcggc 480 ccgacggagc ggcagccgaa ggggccgttc ggcgacctca tcgaatcggc cgcggacaac 540 ctggccggca agggcaggca gctcaacgaa acgctgaaca gtttgtcgca ggcgttgacc 600 gcgctgaacg agggccgggg agacttcgtt gcgatcacgc gaagcctggc gctatttgtc 660 agcgcgctct accagaatga tcaacagttc gttgcgctca acgaaaacct tgccgagttc 720 accgactggt tcaccaaatc cgaccatgac ttggccgaca cggtggaacg gatcgacgac 780 gttctcggca ccgtccgaaa gttcgtgagc gacaacagat ccgtgctggc tgccgatgtc 840 aacaacctcg ccgacgcgac cactacacta gtgcaacccg agccgcggga cggtctggaa 900 accgcgttgc acgtgttgcc gacctacgcc agcaacttca acaaccttta ctatccactg 960 cacagctctc tggtgggcca gttcgtgttc cccaacttcg cgaacccaat tcagctcatt 1020 tgcagcgcta ttcaggccgg cagccgactc ggctatcagg aatccgccga gctgtgcgcg 1080 cagtacttgg caccggttct ggacgctctc aagttcaatt acttgccgtt cggctcaaac 1140 ccgttcagtt cggcggccac tttgcccaag gaggtggctt actccgagga gcggctccgc 1200 ccgccgcccg ggtacaagga caccactgtc ccagggatct tctcgcggga cacaccgttt 1260 tcacacggca accatgaacc gggctgggtc gttgcgcccg ggatgcaggg tatgcaggtt 1320 cagccgttta ccgcgaacat gctcaccccg gaatcgctgg cagagctgct gggtggtccg 1380 gatattgccc ccccgccgcc gggaaccaac ttgcccggac cgccgaatgc gtatgacgag 1440 tccaatccgt tgccgccgcc gtggtacccg cagcccgcgt ccctcccggc tgcgggcgcc 1500 acaggacagc caggcccggg ccag 1524 33 402 PRT Mycobacterium tuberculosis 33 Val Arg Cys Gly Val Ser Ala Gly Ser Ala Asn Gly Lys Pro Asn Arg 1 5 10 15 Trp Thr Leu Arg Cys Gly Val Ser Ala Gly His Arg Gly Ser Val Phe 20 25 30 Leu Leu Ala Val Leu Leu Ala Pro Val Val Leu Thr Ser Cys Thr Trp 35 40 45 Arg Gly Ile Ala Asn Val Pro Leu Pro Val Gly Arg Gly Met Gly Pro 50 55 60 Asp Arg Met Thr Ile Tyr Val Gln Met Pro Asp Thr Leu Ala Leu Asn 65 70 75 80 Thr Asn Ser Arg Val Arg Val Ala Asp Val Trp Val Gly Thr Val Arg 85 90 95 Asp Ile Ser Leu Arg Asn Trp Ile Ala Thr Leu Thr Leu Glu Leu Glu 100 105 110 Pro Thr Val Arg Leu Pro Ala Asn Ala Thr Ala Lys Ile Gly Gln Thr 115 120 125 Ser Leu Leu Gly Thr Gln His Val Glu Leu Ala Ala Pro Pro Ile Pro 130 135 140 Ser Pro Gln Pro Leu Lys Ser Gly Asp Thr Ile Gly Leu Lys Asn Ser 145 150 155 160 Ser Ala Tyr Pro Thr Val Glu Arg Thr Leu Ala Ser Val Ala Leu Ile 165 170 175 Leu Thr Gly Gly Gly Ile Val Asn Leu Asp Val Ile Gln Thr Glu Ile 180 185 190 Leu Asn Ile Leu Asp Gly His Ala Gly Gln Ile Arg Glu Phe Leu Glu 195 200 205 Arg Leu Ala Thr Phe Thr Ala Glu Leu Asn Asn Gln Arg Gly Asp Leu 210 215 220 Thr Arg Ala Ile Asp Ser Thr Asn Gln Leu Leu Thr Ile Ile Ala Asn 225 230 235 240 Arg Asn Asp Thr Leu Asp Arg Val Leu Thr Asp Val Pro Pro Leu Ile 245 250 255 Glu His Phe Ala Asp Thr Gly Gln Leu Phe Ala Asp Ala Thr Glu Ser 260 265 270 Leu Gly Arg Phe Ser Glu Val Ala Asn Arg Ala Leu Ala Ala Thr Arg 275 280 285 Pro Asn Leu His Gln Thr Leu Gln Ser Leu Gln Arg Pro Leu Arg Gln 290 295 300 Leu Glu Arg Ala Ser Pro Tyr Val Val Gly Ala Leu Lys Leu Gly Leu 305 310 315 320 Thr Ala Pro Phe Asn Ile Asp Glu Val Pro Asn Val Ile Arg Gly Asp 325 330 335 Tyr Val Asn Val Ser Ala Thr Phe Asp Val Thr Leu Ser Ala Leu Asp 340 345 350 Asn Ala Leu Leu Ser Gly Thr Gly Ile Ser Gly Met Leu Arg Ala Leu 355 360 365 Glu Gln Ala Trp Gly Arg Asp Pro Asp Thr Met Ile Pro Asp Val Arg 370 375 380 Tyr Thr Pro Asn Pro Asn Asp Ala Pro Gly Gly Pro Leu Val Glu Arg 385 390 395 400 Ala Glu 34 1206 DNA Mycobacterium tuberculosis 34 gtgaggtgcg gcgtgagcgc gggtagcgcg aacggcaagc cgaaccgttg gaccctgagg 60 tgcggcgtga gcgcgggtca ccgtggatcg gtgttcttgc tggcggtctt gctggccccg 120 gtggttttga cttcgtgtac ctggcgtggc atcgccaatg tgccgctgcc ggtcggccgg 180 ggtatgggtc cggatcgcat gacgatctac gtgcagatgc ctgacacgct ggcgctgaac 240 actaacagcc gggtcagggt tgccgacgtc tgggtcggta cggtgcgtga catcagcctg 300 aggaactgga tcgcgaccct gacgctggag ctcgagccga ccgtgcggct accggcaaat 360 gcgaccgcga agatcggcca gaccagcctg ttaggcacac aacatgtcga gctggccgca 420 ccgccaatcc cgtcaccgca gccgctgaaa agcggcgaca ccatcggcct gaagaactcc 480 tcggcctacc ctaccgtcga acggaccttg gccagcgtcg cgttgatcct caccggcggc 540 ggcatcgtca acctcgacgt gattcaaacc gagatcctca acatccttga cggccatgcc 600 ggtcagattc gcgaattcct cgagcggcta gccactttca ccgccgagct gaacaaccaa 660 cgcggcgatc tgactcgcgc aatcgactca accaaccaac tcctgaccat catcgccaac 720 cgcaacgaca cgctggatcg ggtgctcact gacgtcccac cgctgatcga gcatttcgcc 780 gacaccggtc agctgttcgc tgacgccacc gaatccttgg ggcggttcag cgaagtcgcc 840 aaccgggcgc tggcggctac ccggcctaac cttcaccaga cgctgcagtc gttgcagcgg 900 ccgttaaggc aattggaacg ggcttcgccg tatgtggtcg gcgcgttgaa gctaggcctc 960 accgctccgt tcaacatcga cgaggtgcca aacgttatcc gcggcgacta cgtcaacgtg 1020 tccgcgacgt tcgacgtgac gctttctgca ctcgacaacg cactgctgag cggaacgggc 1080 atctcgggaa tgttgcgtgc gctcgagcag gcgtggggac gggatccgga caccatgatc 1140 ccggatgtcc gctacacgcc gaacccgaat gacgcgccgg gcggaccgct ggtggaaagg 1200 gctgag 1206 35 516 PRT Mycobacterium tuberculosis 35 Met Leu Thr Arg Ala Ile Lys Thr Gln Leu Val Leu Leu Thr Val Leu 1 5 10 15 Ala Val Ile Ala Val Val Val Leu Gly Trp Tyr Phe Leu Arg Ile Pro 20 25 30 Ser Leu Val Gly Ile Gly Arg Tyr Thr Leu Tyr Ala Glu Leu Pro Arg 35 40 45 Ser Gly Gly Leu Tyr Arg Thr Ala Asn Val Thr Tyr Arg Gly Ile Thr 50 55 60 Ile Gly Lys Val Thr Gly Val Glu Pro Thr Glu Arg Gly Ala Arg Ala 65 70 75 80 Thr Met Ser Ile Asp Asn Gly Tyr Gln Ile Pro Thr Asp Ala Ser Ala 85 90 95 Asn Val His Ser Val Ser Ala Val Gly Glu Gln Phe Val Asp Leu Val 100 105 110 Ser Thr Arg Thr Ser Gly Pro Tyr Leu Arg His Gly Gln Thr Ile Thr 115 120 125 Thr Thr Thr Val Pro Ser Gln Ile Gly Pro Ala Leu Asp Ala Ala Asn 130 135 140 Arg Gly Leu Ala Val Leu Pro Lys Asp Arg Val Ala Ser Val Leu His 145 150 155 160 Glu Ala Ser Glu Ala Val Gly Gly Leu Gly Ser Ser Leu Asn Arg Leu 165 170 175 Ile Glu Ala Thr Gln Ala Ile Ala His Asp Val Arg Gly Ser Leu Glu 180 185 190 Asp Ile Asp Asp Ile Ile Glu Arg Ser Ala Pro Ile Ile Asp Ser Gln 195 200 205 Val Asn Ser Gly Asn Glu Ile Ala Arg Trp Ala Ala Asn Leu Asn Thr 210 215 220 Leu Ala Ala Gln Thr Ala Gln Thr Asp Pro Ala Val Arg Ser Ile Leu 225 230 235 240 Ala Asn Ala Ala Pro Thr Ala Asp Gln Val Asn Ala Thr Phe Ser Asp 245 250 255 Val Arg Glu Ser Leu Pro Gln Thr Leu Ala Asn Leu Glu Val Val Ile 260 265 270 Asp Met Leu Lys Arg Tyr His Asn Gly Val Glu Gln Ala Leu Val Phe 275 280 285 Leu Pro Gln Ser Gly Ala Ile Ala Gln Ser Val Thr Thr Glu Phe Pro 290 295 300 Gly Gln Ala Gly Leu Gly Val Gly Gly Leu Ala Leu Asn Gln Pro Pro 305 310 315 320 Pro Cys Leu Thr Gly Phe Leu Pro Ala Ser Glu Trp Arg Ser Pro Ala 325 330 335 Asp Thr Ser Thr Ala Pro Leu Pro Lys Gly Thr Tyr Cys Arg Ile Pro 340 345 350 Met Asp Ala Ser Asn Val Val Arg Gly Ala Arg Asn Asn Pro Cys Val 355 360 365 Asp Val Pro Gly Lys Arg Ala Ala Thr Pro Arg Glu Cys Arg Ser Asn 370 375 380 Glu Ala Tyr Val Pro Gly Gly Thr Asn Pro Trp Tyr Gly Asp Pro Asn 385 390 395 400 Gln Met Leu Ser Cys Pro Ala Pro Ala Ala Arg Cys Asp Gln Pro Val 405 410 415 Lys Pro Gly Gln Val Ile Pro Ala Pro Ser Val Asn Asn Gly Ile Asn 420 425 430 Pro Leu Pro Ala Asp Gln Leu Pro Gly Thr Pro Pro Pro Val Asn Asp 435 440 445 Pro Leu Gln Arg Pro Gly Ser Gly Thr Val Gln Cys Asn Gly Gln Gln 450 455 460 Pro Asn Pro Cys Val Tyr Thr Pro Ser Thr Phe Pro Thr Thr Ile Tyr 465 470 475 480 Asp Val Gln Ser Gly Lys Val Val Ala Pro Asp Gly Val Val Tyr Ser 485 490 495 Val Glu Ala Ser Thr His Ala Gly Ala Asp Gly Trp Lys Val Met Leu 500 505 510 Ala Pro Thr Gly 515 36 1548 DNA Mycobacterium tuberculosis 36 atgctgactc gcgctatcaa gacccagctg gtgttgttga cggtgttggc ggtcatcgcg 60 gtggtggtcc ttggttggta tttcctgcgg atacccagcc tggtcggcat cggtcgatac 120 acgctttatg ccgaattgcc tcggtccggg ggtctatacc gaacagccaa cgtcacatat 180 cggggcatca ccatagggaa ggtcaccggc gtcgaaccaa ccgagcgggg cgcgcgagca 240 accatgagca tcgacaatgg ctaccagatc cccaccgacg cctcggccaa tgtgcactca 300 gtgtcggcgg tcggcgagca gttcgttgac ctggtgtcga cccgcaccag cggtccgtat 360 ctgcggcatg ggcagacgat caccacgact acggtcccca gccagattgg cccggcgctg 420 gacgccgcca accgtggatt ggcagtgctg cccaaagacc gggtcgcgtc ggtgctgcac 480 gaggcgtcgg aggccgtggg cgggctggga tcctcactga atcgcctcat cgaagccacc 540 caggcaatcg cccacgatgt caggggcagc ctcgaggaca tcgacgacat catcgagcgt 600 tcggcgccta tcatcgatag ccaggtcaat tccggcaacg agatcgcccg ctgggccgcc 660 aacctcaaca cgctggccgc tcagaccgcg cagaccgatc cggcggtgcg aagcattctg 720 gccaacgcgg caccgactgc cgatcaggtc aacgccacgt tcagcgacgt gcgggagtcg 780 ttgccgcaga cgctggccaa tctcgaggtc gtaatcgata tgctcaagcg ctaccacaac 840 ggcgtcgagc aggcgttggt gttcttgccg cagtccggcg cgatcgccca gtcggttact 900 acagagttcc ccggccaggc cggactgggt gtcggcggcc tggcgctcaa ccaaccaccg 960 ccgtgcctga ccggcttcct gccggcgtcg gagtggcggt cacctgctga caccagcacc 1020 gcaccgctac ccaagggcac ctactgcagg attccgatgg acgcgagcaa tgtggttcgt 1080 ggagcacgca acaacccgtg tgtagacgtg cccggcaagc gggcggcgac cccgcgggaa 1140 tgccgcagca atgaagctta tgtgcccggg ggcaccaatc cctggtatgg ggaccccaac 1200 cagatgctca gctgtcccgc gccggccgcg cgttgtgacc agccggtgaa gccaggccag 1260 gtgatcccgg cgccgtcagt taacaatggc atcaacccgc tgcccgccga tcagctgcca 1320 ggcacacctc caccggtcaa cgatcctttg cagcgacctg ggtcaggcac cgtccagtgc 1380 aatgggcaac aacccaaccc gtgcgtctac accccgagca catttcctac aaccatttac 1440 gacgtgcaga gcggcaaagt cgtagcaccc gacggtgtgg tgtattccgt tgaggcttcg 1500 actcatgccg gagccgacgg atggaaggtg atgctggcac caaccggc 1548 37 790 DNA Mycobacterium tuberculosis 37 ggtgacgttt cgaggctgtg ctgctgccaa gaccccagga agtctcggac gagagactcg 60 ctagcctccg tggtatcggg catccctatc acccctgctc gatcctcaat atcggactaa 120 caaaatacat catcgcgcct gtatacgcga ttacattgca atttatcctt atcacccttc 180 ttagagtgca tatcagtaat agacatatcg cgctcctcgc gccccaggag gcggtcgacg 240 aattcgccgt gcgcaacgac atgagccgtc gctgagcctg aaaacctgca gacaaagcgc 300 gagtgggggc tggcaaaact acaggctcgt tagcagcaag ttgcttcgac gaccatggtg 360 gcaacctcgc cggtcgcgaa ggctctggtc ggcgggcccg aatcgaggcg gtcaggatgc 420 ggcatccgat caccgcccgt cgggcgcgct gttgatgcct gatcgtggtg cctcgccagc 480 gtgactcgag ccaacggctt gaccggtgat gcgcctgtcg gccgccaagg cagcagagca 540 catcgccccg cgctatagga tactagcaag atacatcata gccaatatat gccagtttgc 600 attgctattt accgatcagt tgtccaagca atcgcgtatt ggctatggac atcagcggtt 660 ctgccgcgta cgctcaccaa tgtcaccgat cgtcgacctg tccggggggc cagcgtgcgc 720 cacctcaccc aacggcccag catcgaatcc agctggtgcg ccgcgccatg gtaatcgtgg 780 ccgacaaggc 790 38 265 PRT Mycobacterium tuberculosis 38 Met Val Ile Val Ala Asp Lys Ala Ala Gly Arg Val Ala Asp Pro Val 1 5 10 15 Leu Arg Pro Val Gly Ala Leu Gly Asp Phe Phe Ala Met Thr Leu Asp 20 25 30 Thr Ser Val Cys Met Phe Lys Pro Pro Phe Ala Trp Arg Glu Tyr Leu 35 40 45 Leu Gln Cys Trp Phe Val Ala Arg Val Ser Thr Leu Pro Gly Val Leu 50 55 60 Met Thr Ile Pro Trp Ala Val Ile Ser Gly Phe Leu Phe Asn Val Leu 65 70 75 80 Leu Thr Asp Ile Gly Ala Ala Asp Phe Ser Gly Thr Gly Cys Ala Ile 85 90 95 Phe Thr Val Asn Gln Ser Ala Pro Ile Val Thr Val Leu Val Val Ala 100 105 110 Gly Ala Gly Ala Thr Ala Met Cys Ala Asp Leu Gly Ala Arg Thr Ile 115 120 125 Arg Glu Glu Leu Asp Ala Leu Arg Val Met Gly Ile Asn Pro Ile Gln 130 135 140 Ala Leu Ala Ala Pro Arg Val Leu Ala Ala Thr Thr Val Ser Leu Ala 145 150 155 160 Leu Asn Ser Val Val Thr Ala Thr Gly Leu Ile Gly Ala Phe Phe Cys 165 170 175 Ser Val Phe Leu Met His Val Ser Ala Gly Ala Trp Val Thr Gly Leu 180 185 190 Thr Thr Leu Thr His Thr Val Asp Val Val Ile Ser Met Ile Lys Ala 195 200 205 Thr Leu Phe Gly Leu Met Ala Gly Leu Ile Ala Cys Tyr Lys Gly Met 210 215 220 Ser Val Gly Gly Gly Pro Ala Gly Val Gly Arg Ala Val Asn Glu Thr 225 230 235 240 Val Val Phe Ala Phe Ile Val Leu Phe Val Ile Asn Ile Val Val Thr 245 250 255 Ala Val Gly Ile Pro Phe Met Val Ser 260 265 39 795 DNA Mycobacterium tuberculosis 39 atggtaatcg tggccgacaa ggcggccggt cgggtcgctg atccggtctt gcggccggtg 60 ggcgcgctgg gcgatttctt cgcgatgacg ctcgacacgt ccgtgtgcat gttcaagccg 120 cctttcgcgt ggcgtgaata cctacttcag tgctggttcg tggcgcgggt gtcgacgctg 180 cctggggtgt tgatgacgat cccatgggcg gtgatctcgg ggtttctctt caacgtcttg 240 ctgaccgaca tcggtgccgc ggacttttcc ggcaccggct gtgcgatctt caccgtgaac 300 caaagcgccc cgatcgtcac ggtcttggtg gtcgcgggcg cgggcgccac cgccatgtgc 360 gccgatctgg gtgcgcgcac catccgtgag gaactcgacg cactgcgggt gatgggcatc 420 aacccgatcc aagcgctagc ggctccgcgc gtgctggcgg ccaccacggt gtcgttggcg 480 ctgaattcgg tggtgaccgc gacggggctg atcggcgcgt tcttttgctc ggtgtttctc 540 atgcacgtct cggcgggggc atgggtgacc gggcttacca cgctgaccca caccgtggac 600 gtcgtcattt cgatgatcaa ggcgacgttg ttcgggctga tggccggact gatcgcctgc 660 tataagggca tgtcggtcgg tggcggcccg gccggagtcg gccgggcggt gaacgaaacc 720 gtggtgtttg ccttcatcgt cttgttcgtg atcaacatcg tcgtcaccgc ggtcggcatc 780 ccattcatgg tgtcc 795 40 271 PRT Mycobacterium tuberculosis 40 Met Thr Ala Ala Lys Ala Leu Val Ser Glu Trp Asn Arg Met Gly Ser 1 5 10 15 Gln Met Arg Phe Phe Val Gly Thr Leu Ala Gly Ile Pro Asp Ala Leu 20 25 30 Met His Tyr Arg Gly Glu Leu Leu Arg Val Ile Ala Gln Met Gly Leu 35 40 45 Gly Thr Gly Val Leu Ala Val Ile Gly Gly Thr Val Ala Ile Val Gly 50 55 60 Phe Leu Ala Met Thr Thr Gly Ala Ile Val Ala Val Gln Gly Tyr Asn 65 70 75 80 Gln Phe Ala Ser Val Gly Val Glu Ala Leu Thr Gly Phe Ala Ser Ala 85 90 95 Phe Phe Asn Thr Arg Glu Ile Gln Pro Gly Thr Val Met Val Ala Leu 100 105 110 Ala Ala Thr Val Gly Ala Gly Thr Thr Ala Ala Leu Gly Ala Met Arg 115 120 125 Ile Asn Glu Glu Ile Asp Ala Leu Glu Val Ile Gly Ile Arg Ser Ile 130 135 140 Ser Tyr Leu Ala Ser Thr Arg Val Leu Ala Gly Val Val Val Ala Val 145 150 155 160 Pro Leu Phe Cys Val Gly Leu Met Thr Ala Tyr Leu Ala Ala Arg Val 165 170 175 Gly Thr Thr Ala Ile Tyr Gly Gln Gly Ser Gly Val Tyr Asp His Tyr 180 185 190 Phe Asn Thr Phe Leu Arg Pro Thr Asp Val Leu Trp Ser Ser Val Glu 195 200 205 Val Val Val Val Ala Leu Met Ile Met Leu Val Cys Thr Tyr Tyr Gly 210 215 220 Tyr Ala Ala His Gly Gly Pro Ala Gly Val Gly Glu Ala Val Gly Arg 225 230 235 240 Ala Val Arg Ala Ser Met Val Val Ala Ser Ile Ala Ile Leu Val Met 245 250 255 Thr Leu Ala Ile Tyr Gly Gln Ser Pro Asn Phe His Leu Ala Thr 260 265 270 41 813 DNA Mycobacterium tuberculosis 41 atgacggcag cgaaagccct tgtaagcgaa tggaatcgga tgggatcgca gatgcggttc 60 ttcgtcggca cgctggccgg gattcccgac gccctcatgc actaccgcgg cgagctgctg 120 cgggtgatcg cgcaaatggg gttggggacc ggggttcttg cggtgatcgg tggaacggtc 180 gcgatcgtcg ggttcttggc gatgaccacc ggcgcgatcg tggccgtgca gggctacaac 240 cagttcgctt cggtgggtgt ggaggcgctg accggcttcg cgtcggcctt cttcaacacc 300 cgcgagattc agcccggaac cgtgatggtc gcgctagcgg ccaccgtcgg tgccggtacc 360 accgctgcgc tgggggcgat gcggataaac gaggagatcg acgcgctcga ggtgatcggc 420 atccgcagca tcagctacct ggcgagcacc cgggtgctgg ccggagtggt cgtggccgtc 480 cctctgttct gtgtgggact gatgacggcc tacctggccg cgcgcgtcgg caccaccgcc 540 atctatggcc aggggtcggg cgtgtacgac cactacttca acacgttcct gcgcccgacc 600 gacgtgctct ggtcgtcggt tgaagtcgtc gtggtcgctc tgatgatcat gctggtgtgc 660 acctattacg gctacgccgc acatggcggg ccggccgggg ttggcgaggc ggtcggccgg 720 gccgtgcgtg cctcgatggt cgtcgcgtcg atcgcaatcc ttgtcatgac gctggccatc 780 tacggccagt cgcccaactt tcacctggcg acc 813 42 425 PRT Mycobacterium tuberculosis 42 Met Arg Arg Gly Pro Gly Arg His Arg Leu His Asp Ala Trp Trp Thr 1 5 10 15 Leu Ile Leu Phe Ala Val Ile Gly Val Ala Val Leu Val Thr Ala Val 20 25 30 Ser Phe Thr Gly Ser Leu Arg Ser Thr Val Pro Val Thr Leu Ala Ala 35 40 45 Asp Arg Ser Gly Leu Val Met Asp Ser Gly Ala Lys Val Met Met Arg 50 55 60 Gly Val Gln Val Gly Arg Val Ala Gln Ile Gly Arg Ile Glu Trp Ala 65 70 75 80 Gln Asn Gly Ala Ser Leu Arg Leu Glu Ile Asp Pro Asp Gln Ile Arg 85 90 95 Tyr Ile Pro Ala Asn Val Glu Ala Gln Ile Ser Ala Thr Thr Ala Phe 100 105 110 Gly Ala Lys Phe Val Asp Leu Val Met Pro Gln Asn Pro Ser Arg Ala 115 120 125 Arg Leu Ser Ala Gly Ala Val Leu His Ser Lys Asn Val Ser Thr Glu 130 135 140 Ile Asn Thr Val Phe Glu Asn Val Val Asp Leu Leu Asn Met Ile Asp 145 150 155 160 Pro Leu Lys Leu Asn Ala Val Leu Thr Ala Val Ala Asp Ala Val Arg 165 170 175 Gly Gln Gly Glu Arg Ile Gly Gln Ala Thr Thr Asp Leu Asn Glu Val 180 185 190 Leu Glu Ala Leu Asn Ala Arg Gly Asp Thr Ile Gly Gly Asn Trp Arg 195 200 205 Ser Leu Lys Asn Phe Thr Asp Thr Tyr Asp Ala Ala Ala Gln Asp Ile 210 215 220 Leu Thr Ile Leu Asn Ala Ala Ser Thr Thr Ser Ala Thr Val Val Asn 225 230 235 240 His Ser Thr Gln Leu Asp Ala Leu Leu Leu Asn Ala Ile Gly Leu Ser 245 250 255 Asn Ala Gly Thr Asn Leu Leu Gly Ser Ser Arg Asp Asn Leu Val Gly 260 265 270 Ala Ala Asp Ile Leu Ala Pro Thr Thr Ser Leu Leu Phe Lys Tyr Asn 275 280 285 Pro Glu Tyr Thr Cys Phe Leu Gln Gly Ala Lys Trp Tyr Leu Asp Asn 290 295 300 Gly Gly Tyr Ala Ala Trp Gly Gly Ala Asp Gly Arg Thr Leu Gln Leu 305 310 315 320 Asp Val Ala Leu Leu Phe Gly Asn Asp Pro Tyr Val Tyr Pro Asp Asn 325 330 335 Leu Pro Val Val Ala Ala Lys Gly Gly Pro Gly Gly Arg Pro Gly Cys 340 345 350 Gly Pro Leu Pro Asp Ala Thr His Asn Phe Pro Val Arg Gln Leu Val 355 360 365 Thr Asn Thr Gly Trp Gly Thr Gly Leu Asp Ile Arg Pro Asn Pro Gly 370 375 380 Ile Gly His Pro Cys Trp Ala Asn Tyr Phe Pro Val Thr Arg Ala Val 385 390 395 400 Pro Glu Pro Pro Ser Ile Arg Gln Cys Ile Pro Gly Pro Ala Ile Gly 405 410 415 Pro Asn Pro Ala Ala Gly Glu Gln Pro 420 425 43 1275 DNA Mycobacterium tuberculosis 43 atgagacgcg ggccgggtcg acaccgtttg cacgacgcgt ggtggacgct gatcctgttc 60 gcggtgatcg gggtggctgt cctggtgacg gcggtgtcct tcacgggcag cttgcggtcg 120 actgtgccgg tgacgctggc ggccgaccgc tccgggctgg tgatggactc cggcgccaag 180 gtcatgatgc gcggtgtgca ggtcggccgg gtcgcccaga tcggtcggat cgagtgggcc 240 cagaacgggg cgagcctcag actggagatc gaccccgacc agatccggta catcccggcc 300 aatgtcgagg cacagatcag cgccaccacc gcattcggtg ccaagttcgt cgacctggtg 360 atgccgcaaa acccaagtcg tgcacggctg tccgctgggg cggtactgca ttcgaagaac 420 gtcagcacgg aaatcaacac cgtcttcgaa aacgtcgtcg acctgctcaa catgatcgac 480 ccgctgaaac tgaacgccgt gctgaccgcg gtcgccgacg ccgttcgcgg gcaaggtgaa 540 cggataggcc aggccaccac cgacctcaac gaggtgctgg aggcactcaa cgcacgcggc 600 gacaccatcg gcggcaactg gcgatcgctc aagaacttca ccgacaccta tgacgcggcc 660 gcccaagaca tcctgacgat cctgaacgcc gccagcacca ccagtgcgac cgtcgtgaat 720 cattcgacgc agctggatgc cttgctactc aacgccatcg gactatccaa cgctggcacc 780 aacctgcttg gcagcagccg agacaatctc gtcggcgcgg ccgacatcct ggcgccgacc 840 acgagcctgc tgttcaagta caaccccgaa tacacctgct tcctgcaggg cgccaagtgg 900 tatctcgaca acggcggcta tgcggcctgg ggcggggccg acgggcgcac gctacaactc 960 gatgtggcgc tactgttcgg caacgacccc tatgtctatc cggacaacct gccggttgtc 1020 gcggccaagg ggggtcccgg cggaaggccg ggatgcgggc cattgccgga tgccacccac 1080 aacttcccgg tgcgccagct ggtcaccaac accggatggg gaaccgggct ggacatccgg 1140 cccaaccccg gcatcgggca tccctgctgg gccaactact tcccggtgac ccgcgcggtg 1200 cccgagccgc cgtcgatccg tcagtgcatc cccgggccgg cgatcgggcc caaccccgcg 1260 gcgggggagc agcca 1275 44 342 PRT Mycobacterium tuberculosis 44 Met Arg Glu Asn Leu Gly Gly Val Val Val Arg Leu Gly Val Phe Leu 1 5 10 15 Ala Val Cys Leu Leu Thr Ala Phe Leu Leu Ile Ala Val Phe Gly Glu 20 25 30 Val Arg Phe Gly Asp Gly Lys Thr Tyr Tyr Ala Glu Phe Ala Asn Val 35 40 45 Ser Asn Leu Arg Thr Gly Lys Leu Val Arg Ile Ala Gly Val Glu Val 50 55 60 Gly Lys Val Thr Arg Ile Ser Ile Asn Pro Asp Ala Thr Val Arg Val 65 70 75 80 Gln Phe Thr Ala Asp Asn Ser Val Thr Leu Thr Arg Gly Thr Arg Ala 85 90 95 Val Ile Arg Tyr Asp Asn Leu Phe Gly Asp Arg Tyr Leu Ala Leu Glu 100 105 110 Glu Gly Ala Gly Gly Leu Ala Val Leu Arg Pro Gly His Thr Ile Pro 115 120 125 Leu Ala Arg Thr Gln Pro Ala Leu Asp Leu Asp Ala Leu Ile Gly Gly 130 135 140 Phe Lys Pro Leu Phe Arg Ala Leu Asn Pro Glu Gln Val Asn Ala Leu 145 150 155 160 Ser Glu Gln Leu Leu His Ala Phe Ala Gly Gln Gly Pro Thr Ile Gly 165 170 175 Ser Leu Leu Ala Gln Ser Ala Ala Val Thr Asn Thr Leu Ala Asp Arg 180 185 190 Asp Arg Leu Ile Gly Gln Val Ile Thr Asn Leu Asn Val Val Leu Gly 195 200 205 Ser Leu Gly Ala His Thr Asp Arg Leu Asp Gln Ala Val Thr Ser Leu 210 215 220 Ser Ala Leu Ile His Arg Leu Ala Gln Arg Lys Thr Asp Ile Ser Asn 225 230 235 240 Ala Val Ala Tyr Thr Asn Ala Ala Ala Gly Ser Val Ala Asp Leu Leu 245 250 255 Ser Gln Ala Arg Ala Pro Leu Ala Lys Val Val Arg Glu Thr Asp Arg 260 265 270 Val Ala Gly Ile Ala Ala Ala Asp His Asp Tyr Leu Asp Asn Leu Leu 275 280 285 Asn Thr Leu Pro Asp Lys Tyr Gln Ala Leu Val Arg Gln Gly Met Tyr 290 295 300 Gly Asp Phe Phe Ala Phe Tyr Leu Cys Asp Val Val Leu Lys Val Asn 305 310 315 320 Gly Lys Gly Gly Gln Pro Val Tyr Ile Lys Leu Ala Gly Gln Asp Ser 325 330 335 Gly Arg Cys Ala Pro Lys 340 45 1026 DNA Mycobacterium tuberculosis 45 atgagggaga acctgggggg cgtcgtggtg cgcctcggcg tcttcctggc ggtatgcctg 60 ctgacggcgt tcctgctgat tgccgtcttc ggggaggtgc gcttcggcga cggcaagacc 120 tactacgccg agttcgccaa cgtgtccaat ctgcgaacgg gcaagctggt gcgcatcgcc 180 ggcgtcgagg tcggcaaggt caccaggatc tccatcaacc ccgacgcgac ggtgcgggtg 240 cagttcaccg ccgacaactc ggtcaccctc acgcggggca cccgggcggt gatccgctac 300 gacaacctgt tcggtgaccg ctatttggcg ctggaggaag gggccggcgg actcgccgtt 360 cttcgtcccg gtcacacgat tccgttggcg cgcacccaac cggcgttgga tctggatgcc 420 ctgatcggtg gattcaagcc gctgtttcgt gcgctgaacc ccgagcaggt caacgcgctg 480 agcgaacagt tgctgcacgc gtttgccgga caggggccca cgatcgggtc attgctggcc 540 cagtccgcgg ccgtgaccaa caccctggcc gaccgtgatc ggctgatcgg gcaggtgatc 600 accaacctca acgtggtgct gggctcgctg ggcgctcaca ccgatcggtt ggaccaggcg 660 gtgacgtcgc tatcagcgtt gattcaccgg ctcgcgcaac gcaagaccga catctccaac 720 gccgtggcct acaccaacgc cgccgccggc tcggtcgccg atctgctgtc gcaggctcgc 780 gcgccgttgg cgaaggtggt tcgcgagacc gatcgggtgg ccggcatcgc ggccgccgac 840 cacgactacc tcgacaatct gctcaacacg ctgccggaca aataccaggc gctggtccgc 900 cagggtatgt acggcgactt cttcgccttc tacctgtgcg acgtcgtgct caaggtcaac 960 ggcaagggcg gccagccggt gtacatcaag ctggccggtc aggacagcgg gcggtgcgcg 1020 ccgaaa 1026 46 410 PRT Mycobacterium tuberculosis 46 Met Lys Ser Phe Ala Glu Arg Asn Arg Leu Ala Ile Gly Thr Val Gly 1 5 10 15 Ile Val Val Val Ala Ala Val Ala Leu Ala Ala Leu Gln Tyr Gln Arg 20 25 30 Leu Pro Phe Phe Asn Gln Gly Thr Arg Val Ser Ala Tyr Phe Ala Asp 35 40 45 Ala Gly Gly Leu Arg Thr Gly Asn Thr Val Glu Val Ser Gly Tyr Pro 50 55 60 Val Gly Lys Val Ser Ser Ile Ser Leu Asp Gly Pro Gly Val Leu Val 65 70 75 80 Glu Phe Lys Val Asp Thr Asp Val Arg Leu Gly Asn Arg Thr Glu Val 85 90 95 Ala Ile Lys Thr Lys Gly Leu Leu Gly Ser Lys Phe Leu Asp Val Thr 100 105 110 Pro Arg Gly Asp Gly Arg Leu Asp Ser Pro Ile Pro Ile Glu Arg Thr 115 120 125 Thr Ser Pro Tyr Gln Leu Pro Asp Ala Leu Gly Asp Leu Ala Ala Thr 130 135 140 Ile Ser Gly Leu His Thr Glu Arg Leu Ser Glu Ser Leu Ala Thr Leu 145 150 155 160 Ala Gln Thr Phe Ala Asp Thr Pro Ala His Phe Arg Asn Ala Ile His 165 170 175 Gly Val Ala Arg Leu Ala Gln Thr Leu Asp Glu Arg Asp Asn Gln Leu 180 185 190 Arg Ser Leu Leu Ala Asn Ala Ala Lys Ala Thr Gly Val Leu Ala Asn 195 200 205 Arg Thr Asp Gln Ile Val Gly Leu Val Arg Asp Thr Asn Val Val Leu 210 215 220 Ala Gln Leu Arg Thr Gln Ser Ala Ala Leu Asp Arg Ile Trp Ala Asn 225 230 235 240 Ile Ser Ala Val Ala Glu Gln Leu Arg Gly Phe Ile Ala Glu Asn Arg 245 250 255 Gln Gln Leu Arg Pro Ala Leu Asp Lys Leu Asn Gly Val Leu Ala Ile 260 265 270 Val Glu Asn Arg Lys Glu Arg Val Arg Gln Ala Ile Pro Leu Ile Asn 275 280 285 Thr Tyr Val Met Ser Leu Gly Glu Ser Leu Ser Ser Gly Pro Phe Phe 290 295 300 Lys Ala Tyr Val Val Asn Leu Leu Pro Gly Gln Phe Val Gln Pro Phe 305 310 315 320 Ile Ser Ala Ala Phe Ser Asp Leu Gly Leu Asp Pro Ala Thr Leu Leu 325 330 335 Pro Ser Gln Leu Thr Asp Pro Pro Thr Gly Gln Pro Gly Thr Pro Pro 340 345 350 Leu Pro Met Pro Tyr Pro Arg Thr Gly Gln Gly Gly Glu Pro Arg Leu 355 360 365 Thr Leu Pro Asp Ala Ile Thr Gly Asn Pro Gly Asp Pro Arg Tyr Pro 370 375 380 Tyr Arg Pro Glu Pro Pro Ala Pro Pro Pro Gly Gly Pro Pro Pro Gly 385 390 395 400 Pro Pro Ala Gln Gln Pro Gly Asp Gln Pro 405 410 47 1230 DNA Mycobacterium tuberculosis 47 atgaaatcct tcgccgaacg caaccgtctg gccatcggca cagtcggcat cgtcgtcgtc 60 gccgccgttg cgctggccgc gctgcaatac cagcggctgc cgtttttcaa ccagggcacc 120 agggtctccg cctatttcgc cgacgccggc gggctgcgca ccggcaacac cgtcgaggtc 180 tccggctatc cggtgggaaa agtgtccagc atctcgctcg acggaccggg cgtgctggtg 240 gagttcaagg tcgacaccga cgtccgactc ggaaaccgca ccgaagtggc aatcaaaacc 300 aagggcttgt tgggcagcaa gttcctcgac gtcacccccc gcggggacgg ccgactcgat 360 tctccgatcc cgatcgagcg gaccacgtcg ccctaccaac tgcccgacgc ccttggcgat 420 ttggccgcca cgatcagcgg gttgcacacc gagcggctgt ccgaatcgct ggccaccctg 480 gcgcagacct ttgccgatac gccggcgcac ttccgcaacg ccatacacgg ggtggcccgg 540 ctcgcccaaa ccctcgatga gcgcgacaac caactgcgca gcctgctggc caacgcggcc 600 aaagccaccg gggtgctggc caaccgcacc gaccagatcg tcggcctggt gcgcgacacg 660 aatgtggtct tggcgcagct gcgcacccaa agcgccgccc tggaccggat ctgggcgaac 720 atctcggcgg tggccgaaca actgcggggc ttcatcgctg agaaccgcca gcagctgcgc 780 ccggcgctgg acaagctcaa cggggtgctg gctatcgtcg aaaaccgcaa agagcgtgtg 840 cggcaggcca tcccgctgat caacacctat gtcatgtcgc tgggtgagtc gctgtcgtcg 900 ggcccgttct tcaaggcata cgtggtgaac ctgctgccgg gtcagttcgt gcaaccgttc 960 atcagcgccg cgttctccga cctggggctc gacccggcca cgttgctgcc gtcgcagctg 1020 accgacccac cgaccggtca acccggaacc ccgccgttgc cgatgcccta cccgcgcacg 1080 ggccagggcg gtgagccgcg gctgacgctg cccgacgcga tcaccggcaa tcccggcgat 1140 ccgcgctatc cgtaccggcc ggagccgccc gcgccgccgc ccggcgggcc gccgcccggc 1200 ccgcccgcgc agcagccggg agaccaaccg 1230 48 423 PRT Mycobacterium tuberculosis 48 Val Thr Thr Lys Leu Arg Arg Ala Arg Ser Val Leu Ala Thr Ala Leu 1 5 10 15 Val Leu Val Ala Gly Val Ile Leu Ala Met Arg Thr Ala Asp Ala Ala 20 25 30 Ala Arg Thr Thr Val Val Ala Tyr Phe Asp Asn Ser Asn Gly Val Phe 35 40 45 Ala Gly Asp Asp Val Leu Ile Arg Gly Val Pro Val Gly Lys Ile Val 50 55 60 Lys Ile Glu Pro Gln Pro Leu Arg Ala Lys Ile Ser Phe Trp Phe Asp 65 70 75 80 Arg Lys Tyr Arg Val Pro Ala Asp Ala Ala Ala Ala Ile Leu Ser Pro 85 90 95 Gln Leu Val Thr Gly Arg Ala Ile Gln Leu Thr Pro Pro Tyr Ala Gly 100 105 110 Gly Pro Thr Met Ala Asp Gly Thr Val Ile Pro Gln Glu Arg Thr Val 115 120 125 Val Pro Val Glu Trp Asp Asp Leu Arg Ala Gln Leu Gln Arg Leu Thr 130 135 140 Ala Leu Leu Gln Pro Thr Arg Pro Gly Gly Val Ser Thr Leu Gly Ala 145 150 155 160 Leu Ile Asn Thr Ala Ala Asp Asn Leu Arg Gly Gln Gly Ala Thr Ile 165 170 175 Arg Asp Thr Ile Ile Lys Leu Ser Gln Ala Ile Ser Ala Leu Gly Asp 180 185 190 His Ser Lys Asp Ile Phe Ser Thr Val Thr Asn Leu Ser Thr Leu Val 195 200 205 Thr Ala Leu His Asp Ser Ala Asp Leu Leu Glu Arg Leu Asn His Asn 210 215 220 Leu Ala Ala Val Thr Ser Leu Leu Ala Asp Gly Pro Asp Lys Ile Gly 225 230 235 240 Gln Ala Ala Glu Asp Leu Asn Ala Val Val Ala Asp Val Gly Ser Phe 245 250 255 Ala Ala Glu His Arg Glu Ala Ile Gly Thr Ala Ser Asp Lys Leu Ala 260 265 270 Ser Ile Thr Thr Ala Leu Val Asp Ser Leu Asp Asp Ile Lys Gln Thr 275 280 285 Leu His Ile Ser Pro Thr Val Leu Gln Asn Phe Asn Asn Ile Phe Glu 290 295 300 Pro Ala Asn Gly Ala Leu Thr Gly Ala Leu Ala Gly Asn Asn Met Ala 305 310 315 320 Asn Pro Ile Ala Phe Leu Cys Gly Ala Ile Gln Ala Ala Ser Arg Leu 325 330 335 Gly Gly Glu Gln Ala Ala Lys Leu Cys Val Gln Tyr Leu Ala Pro Ile 340 345 350 Val Lys Asn Arg Gln Tyr Asn Tyr Pro Pro Leu Gly Ala Asn Leu Phe 355 360 365 Val Gly Ala Gln Ala Arg Pro Asn Glu Val Thr Tyr Ser Glu Asp Trp 370 375 380 Leu Arg Pro Asp Tyr Val Ala Pro Val Ala Asp Thr Pro Pro Asp Pro 385 390 395 400 Ala Ala Ala Val Thr Val Asp Pro Ala Thr Gly Leu Arg Gly Met Met 405 410 415 Met Pro Pro Gly Gly Gly Ser 420 49 1269 DNA Mycobacterium tuberculosis 49 gtgacaacga aactcagacg tgcccgctcg gtgttggcga ccgccctggt gctggtcgcg 60 ggcgtgatcc tggccatgcg caccgccgac gccgccgccc gcacgaccgt ggtcgcctac 120 ttcgacaaca gcaacggtgt gttcgccggt gacgacgtgc tcattcgggg cgtgccggtg 180 ggcaagatcg tcaagatcga accgcaaccg ctgcgcgcca agatttcgtt ctggttcgac 240 cgcaaatacc gagtccccgc cgatgccgcc gcggcgatcc tgtcgccgca actggtgacc 300 ggccgggcca tccagctgac accgccgtat gccggcgggc cgaccatggc cgacggcaca 360 gtaatcccgc aagagcgcac cgtggtgccg gtggagtggg acgacttgcg ggcgcaactt 420 cagcggctga ccgcattgct gcagcccacc cggccgggcg gcgtcagcac gctgggtgcg 480 ctcatcaata ctgccgccga caacctgcgc gggcaaggcg ccaccatccg cgacaccatc 540 atcaaactgt cacaagcgat ttcggctctc ggtgaccaca gcaaagacat cttctccacc 600 gtgacgaacc tgtcgacgct ggtcacggcg ctgcatgaca gcgctgacct gctcgaacgg 660 ctcaaccaca acctggccgc ggtgacctcg ctgctggccg atggcccgga caagatcggt 720 caggcagccg aggacctcaa cgcggtcgta gccgacgtcg gcagcttcgc cgccgagcac 780 cgcgaggcga tcggcaccgc atcagacaag ctcgcgtcaa tcaccaccgc gctggtcgac 840 agcctcgacg acatcaagca gacgctgcat atcagcccga cggtgttgca gaacttcaac 900 aacatcttcg aaccggccaa cggcgcgctg accggcgcgc tggcgggcaa caacatggcc 960 aacccaatcg ccttcctgtg cggcgcgatc caggctgcct cccggctggg cggcgagcaa 1020 gcggccaaat tgtgcgtgca atacctggcg ccgatcgtga agaaccgcca gtacaactac 1080 ccgccgctgg gggcgaacct gttcgtcggg gcgcaggcca ggcctaacga ggtcacctac 1140 agcgaggact ggctgcggcc cgattacgtt gcaccagttg cggacacgcc gccagatccg 1200 gccgcggccg tgaccgtcga tcccgcgacc ggcctgcgcg gcatgatgat gccgccgggg 1260 ggtggctcg 1269 50 377 PRT Mycobacterium tuberculosis 50 Val Arg Ile Gly Leu Thr Leu Val Met Ile Ala Ala Val Val Ala Ser 1 5 10 15 Cys Gly Trp Arg Gly Leu Asn Ser Leu Pro Leu Pro Gly Thr Gln Gly 20 25 30 Asn Gly Pro Gly Ser Phe Ala Val Gln Ala Gln Leu Pro Asp Val Asn 35 40 45 Asn Ile Gln Pro Asn Ser Arg Val Arg Val Ala Asp Val Thr Val Gly 50 55 60 His Val Thr Lys Ile Glu Arg Gln Gly Trp His Ala Leu Val Thr Met 65 70 75 80 Arg Leu Asp Gly Asp Val Asp Leu Pro Ala Asn Ala Thr Ala Lys Ile 85 90 95 Gly Thr Thr Ser Leu Leu Gly Ser Tyr His Ile Glu Leu Ala Pro Pro 100 105 110 Lys Gly Glu Ala Arg Gln Gly Lys Leu Arg Asp Gly Ser Leu Ile Ala 115 120 125 Leu Ser His Gly Ser Ala Tyr Pro Ser Thr Glu Gln Thr Leu Ala Ala 130 135 140 Leu Ser Leu Val Leu Asn Gly Gly Gly Leu Gly Gln Val Gln Asp Ile 145 150 155 160 Thr Glu Ala Leu Ser Thr Ala Phe Ala Gly Arg Glu His Asp Leu Arg 165 170 175 Gly Leu Ile Gly Gln Leu Asp Thr Phe Thr Ala Tyr Leu Asn Asn Gln 180 185 190 Ser Gly Asp Ile Ile Ala Ala Thr Asp Ser Leu Asn Arg Leu Val Gly 195 200 205 Lys Phe Ala Asp Gln Gln Pro Val Phe Asp Arg Ala Leu Ala Thr Ile 210 215 220 Pro Asp Ala Leu Ala Val Leu Ala Asp Glu Arg Asp Thr Leu Val Glu 225 230 235 240 Ala Ala Glu Gln Leu Ser Lys Phe Ser Ala Leu Thr Val Asp Ser Val 245 250 255 Asn Lys Thr Thr Ala Asn Leu Val Thr Glu Leu Arg Gln Leu Gly Pro 260 265 270 Val Leu Glu Ser Leu Ala Asn Ser Gly Pro Ala Leu Thr Arg Ser Leu 275 280 285 Ser Leu Leu Ala Thr Phe Pro Phe Pro Asn Glu Thr Phe Gln Asn Phe 290 295 300 Gln Arg Gly Glu Tyr Ala Asn Leu Thr Ala Ile Val Asp Leu Thr Leu 305 310 315 320 Ser Arg Ile Asp Gln Gly Leu Leu Thr Gly Thr Arg Trp Glu Cys His 325 330 335 Leu Thr Gln Leu Glu Leu Gln Trp Gly Arg Thr Ile Gly Gln Phe Pro 340 345 350 Ser Pro Cys Thr Ala Gly Tyr Arg Gly Thr Pro Gly Asn Pro Leu Thr 355 360 365 Ile Ala Tyr Arg Trp Asp Gln Gly Pro 370 375 51 1131 DNA Mycobacterium tuberculosis 51 gtgaggatcg gcctgaccct ggtgatgatc gcggccgtgg tagcgagctg cggctggcgc 60 gggctgaatt cgctgccgct gcccggcacg cagggcaacg gcccggggtc cttcgcggtc 120 caggcgcagc tgccggatgt caacaacatc cagccgaact cgcgggtgcg ggttgccgac 180 gtgacggtcg gccacgtcac gaaaatcgag cgccaaggct ggcacgcgtt ggtgaccatg 240 cggctggatg gcgacgtcga tttgcccgcc aacgcaacgg ccaagatcgg caccaccagc 300 ctgctgggtt cctaccacat cgagctggcg ccaccgaaag gcgaagcgcg gcaaggcaag 360 ctgcgcgacg gttcactcat tgcgctgtca cacggtagcg cctacccaag caccgagcag 420 acgctggcag cgctgtcgct ggtgctcaac ggcggcggac tgggccaggt tcaagacatc 480 accgaggcgt tgagcaccgc gtttgccggc cgtgagcacg atctgcgcgg gctgattggg 540 cagctggaca ccttcaccgc atacctcaac aaccagtccg gtgacatcat cgcggccacc 600 gacagcctca accgcctcgt cggcaagttc gccgaccagc aacccgtctt cgatcgggcc 660 ctggccacca tccccgacgc gctcgcggtg ctggccgatg agcgggacac gctcgtcgag 720 gctgccgagc agctgagcaa gttcagcgcc ctgaccgtcg actcggtcaa caagaccacc 780 gcgaacctgg tcaccgaact gcggcaactc ggaccggtgt tggagtcgct ggccaattcc 840 ggtccggcgc tgacccgatc gctgtccctg ctggccacgt tcccgttccc gaacgagacg 900 ttccaaaatt tccagcgcgg cgaatacgcc aacctgaccg cgatcgtcga cctcacgctc 960 agccgcatcg accagggcct gttgaccggc acccgctggg agtgtcatct gacccagctc 1020 gagctgcagt ggggtcgcac cattgggcag ttccccagcc cgtgtaccgc gggctatcgg 1080 ggtaccccgg gcaatccgct gacgatcgcc taccgctggg atcaggggcc c 1131 52 437 PRT Mycobacterium tuberculosis 52 Met Leu His Leu Pro Arg Arg Val Ile Val Gln Leu Ala Val Phe Thr 1 5 10 15 Val Ile Ala Val Gly Val Leu Ala Ile Thr Phe Leu His Phe Val Arg 20 25 30 Leu Pro Ala Met Leu Phe Gly Val Gly Arg Tyr Thr Val Thr Met Glu 35 40 45 Leu Val Glu Ala Gly Gly Leu Tyr Arg Thr Gly Asn Val Thr Tyr Arg 50 55 60 Gly Phe Glu Val Gly Arg Val Ala Ala Val Arg Leu Thr Asp Thr Gly 65 70 75 80 Val Gln Ala Val Leu Ala Leu Lys Ser Gly Ile Asp Ile Pro Ser Asp 85 90 95 Leu Lys Ala Glu Val His Ser His Thr Ala Ile Gly Glu Thr Tyr Val 100 105 110 Glu Leu Leu Pro Arg Asn Ala Ala Ser Pro Pro Leu Lys Asn Gly Asp 115 120 125 Val Ile Ala Leu Ala Asp Thr Ser Val Pro Pro Asp Ile Asn Asp Leu 130 135 140 Leu Ser Ala Ala Asn Thr Ala Leu Glu Ala Ile Pro His Glu Asn Leu 145 150 155 160 Gln Thr Val Ile Asp Glu Ser Tyr Thr Ala Val Ala Gly Leu Gly Leu 165 170 175 Glu Leu Ser Arg Leu Ile Lys Gly Ser Ala Glu Leu Ala Ile Asp Ala 180 185 190 Arg Ala Asn Leu Asp Pro Leu Val Ala Leu Ile Asp Arg Ala Gly Pro 195 200 205 Val Leu Asp Ser Gln Thr His Thr Ser Asp Ala Ile Ala Ala Trp Ala 210 215 220 Ala Gln Leu Ala Ala Val Thr Gly Gln Leu Gln Thr His Asp Ser Ala 225 230 235 240 Val Gly Asp Leu Ile Asp Arg Gly Gly Pro Ala Leu Gly Glu Thr Arg 245 250 255 Gln Leu Leu Glu Arg Leu Gln Pro Thr Val Pro Ile Leu Leu Ala Asn 260 265 270 Leu Val Ser Val Gly Gln Val Ala Leu Thr Tyr His Asn Asp Ile Glu 275 280 285 Gln Leu Leu Val Val Phe Pro Met Ala Ile Ala Ala Glu Gln Ala Gly 290 295 300 Ile Leu Ala Asn Leu Asn Thr Lys Gln Ala Tyr Arg Gly Gln Tyr Leu 305 310 315 320 Ser Phe Asn Leu Asn Leu Asn Leu Pro Pro Pro Cys Thr Thr Gly Phe 325 330 335 Leu Pro Ala Gln Gln Arg Arg Ile Pro Thr Phe Glu Asp Tyr Pro Asp 340 345 350 Arg Pro Ala Gly Asp Leu Tyr Cys Arg Val Pro Gln Asp Ser Pro Phe 355 360 365 Asn Val Arg Gly Ala Arg Asn Ile Pro Cys Glu Thr Val Pro Gly Lys 370 375 380 Arg Ala Pro Thr Val Lys Leu Cys Glu Ser Asp Ala Pro Tyr Leu Pro 385 390 395 400 Leu Asn Asp Gly Tyr Asn Trp Lys Gly Asp Pro Asn Ala Thr Val Pro 405 410 415 Gly Leu Gly Ser Gly Gln Asp Ile Pro Gln Thr Trp Gln Thr Met Leu 420 425 430 Leu Pro Pro Gly Ser 435 53 1311 DNA Mycobacterium tuberculosis 53 atgctgcatc taccgcgccg agtgatcgtt cagctggccg tctttaccgt gatcgcggtg 60 ggcgtgctgg ccatcacgtt cctgcatttc gtgaggctgc cggcgatgct tttcggcgtc 120 ggccgctaca cggtgacgat ggagctggtc gaagccggtg ggctgtatcg caccggcaat 180 gtcacctacc gcggctttga ggtgggccgg gtggcagcgg tgcggctcac cgacaccggg 240 gtgcaagcgg tgctggccct gaaatcgggc atcgatatcc cgtcggacct caaggccgag 300 gtgcacagcc acaccgcgat cggcgaaacc tacgtcgagt tgttgccgcg caacgccgcc 360 tcgccgccac tgaagaacgg cgatgtcatt gcgctggccg acacctcggt gccgcccgac 420 atcaacgacc tgctcagcgc ggccaacacc gcattggagg caatacctca cgagaacctg 480 cagaccgtca tcgacgagtc gtacaccgcg gtggccgggt tagggctcga actttcccgg 540 ctgatcaagg gctcggcgga actggcgatc gatgctcgcg cgaatctcga tccgctggtg 600 gcgctgatcg accgggcagg accggtgctg gattcgcaga cccacacctc ggatgcgatc 660 gcggcctggg cggcacagct ggccgcagtc accggccaat tgcagacaca cgactcggcg 720 gtcggcgatc tcatcgaccg gggcggtccg gcgttggggg agacgcgcca actgctcgag 780 cggctacaac ccaccgtgcc catcctgctg gccaacctgg tcagcgtcgg ccaggtcgca 840 ctcacctatc acaacgacat cgaacagctg ctggtggtgt tccccatggc catcgccgcc 900 gaacaggccg gcatcctggc caacctcaac accaagcagg cctaccgggg ccagtatctg 960 agcttcaacc tcaacctgaa cctgccgccg ccgtgcacca ccggctttct gccggcccag 1020 cagcggcgca ttcccacgtt cgaggactac ccggatcgcc cggccggtga tctgtactgc 1080 cgggtgcccc aggattcgcc gtttaacgtg cgcggcgccc gcaacatccc ctgtgaaacc 1140 gtgccgggca agcgcgcacc caccgtgaag ttatgcgaga gcgacgcgcc atacctgccg 1200 ctgaacgacg gctacaactg gaagggcgac cccaacgcca cggtgccggg tttggggtcc 1260 ggccaggaca tcccgcagac atggcaaacg atgctgctgc cgccgggcag c 1311 54 380 DNA Mycobacterium tuberculosis 54 ttgatgtcag gctgattcat gggtcgcgca tggcgccttt ctgccgaaca aacgcatggc 60 ccgagcgggc gacgggaatc gaacccgcgt cgctagtttg gaagactagg gctctaccat 120 tgagctacgc ccgcatgtat ttagtcgagc gcgactgtac gtggtgacag acatcaaatc 180 taatcggagt cgttttgaga ccttcccgtg aggtctcaag aggtcattgc ggtgccggtg 240 tcgccgggcc gtaggatcgc gaggtcagcg cggggtgtag cgcagcttgg tagcgcatcc 300 gctttgggag cggaaggccg caggttcaaa tcctgtcacc ccgaccagcc gaccgccgtt 360 atcgactacc aaggagcaca 380 55 466 PRT Mycobacterium tuberculosis 55 Val Lys Ser Thr Val Glu Gln Leu Ser Pro Thr Arg Val Arg Ile Asn 1 5 10 15 Val Glu Val Pro Phe Ala Glu Leu Glu Pro Asp Phe Gln Arg Ala Tyr 20 25 30 Lys Glu Leu Ala Lys Gln Val Arg Leu Pro Gly Phe Arg Pro Gly Lys 35 40 45 Ala Pro Ala Lys Leu Leu Glu Ala Arg Ile Gly Arg Glu Ala Met Leu 50 55 60 Asp Gln Ile Val Asn Asp Ala Leu Pro Ser Arg Tyr Gly Gln Ala Val 65 70 75 80 Ala Glu Ser Asp Val Gln Pro Leu Gly Arg Pro Asn Ile Glu Val Thr 85 90 95 Lys Lys Glu Tyr Gly Gln Asp Leu Gln Phe Thr Ala Glu Val Asp Ile 100 105 110 Arg Pro Lys Ile Ser Pro Pro Asp Leu Ser Ala Leu Thr Val Ser Val 115 120 125 Asp Pro Ile Glu Ile Gly Glu Asp Asp Val Asp Ala Glu Leu Gln Ser 130 135 140 Leu Arg Thr Arg Phe Gly Thr Leu Thr Ala Val Asp Arg Pro Val Ala 145 150 155 160 Val Gly Asp Val Val Ser Ile Asp Leu Ser Ala Thr Val Asp Gly Glu 165 170 175 Asp Ile Pro Asn Ala Ala Ala Glu Gly Leu Ser His Glu Val Gly Ser 180 185 190 Gly Arg Leu Ile Ala Gly Leu Asp Asp Ala Val Val Gly Leu Ser Ala 195 200 205 Asp Glu Ser Arg Val Phe Thr Ala Lys Leu Ala Ala Gly Glu His Ala 210 215 220 Gly Gln Glu Ala Gln Val Thr Val Thr Val Arg Ser Val Lys Glu Arg 225 230 235 240 Glu Leu Pro Glu Pro Asp Asp Glu Phe Ala Gln Leu Ala Ser Glu Phe 245 250 255 Asp Ser Ile Asp Glu Leu Arg Ala Ser Leu Ser Asp Gln Val Arg Gln 260 265 270 Ala Lys Arg Ala Gln Gln Ala Glu Gln Ile Arg Asn Ala Thr Ile Asp 275 280 285 Ala Leu Leu Glu Gln Val Asp Val Pro Leu Pro Glu Ser Tyr Val Gln 290 295 300 Ala Gln Phe Asp Ser Val Leu His Ser Ala Leu Ser Gly Leu Asn His 305 310 315 320 Asp Glu Ala Arg Phe Asn Glu Leu Leu Val Glu Gln Gly Ser Ser Arg 325 330 335 Ala Ala Phe Asp Ala Glu Ala Arg Thr Ala Ser Glu Lys Asp Val Lys 340 345 350 Arg Gln Leu Leu Leu Asp Ala Leu Ala Asp Glu Leu Gln Val Gln Val 355 360 365 Gly Gln Asp Asp Leu Thr Glu Arg Leu Val Thr Thr Ser Arg Gln Tyr 370 375 380 Gly Ile Glu Pro Gln Gln Leu Phe Gly Tyr Leu Gln Glu Arg Asn Gln 385 390 395 400 Leu Pro Thr Met Phe Ala Asp Val Arg Arg Glu Leu Ala Ile Arg Ala 405 410 415 Ala Val Glu Ala Ala Thr Val Thr Asp Ser Asp Gly Asn Thr Ile Asp 420 425 430 Thr Ser Glu Phe Phe Gly Lys Arg Val Ser Ala Gly Glu Ala Glu Glu 435 440 445 Ala Glu Pro Ala Asp Glu Gly Ala Ala Arg Ala Ala Ser Asp Glu Ala 450 455 460 Thr Thr 465 56 1398 DNA Mycobacterium tuberculosis 56 gtgaagagca ccgtcgagca gttgagcccc acccgggttc gtatcaacgt ggaggtgcca 60 ttcgccgagc ttgagccgga tttccagcgg gcctacaaag agctggccaa acaggtgcgg 120 ctgcccggct tccggcccgg gaaggcgccg gccaaactac tcgaagcccg catcggccgg 180 gaggccatgc tggatcaaat cgtcaacgat gcgctgccca gccggtacgg acaggcggtg 240 gccgagtcgg atgtccaacc gctcggccgg cccaacatcg aggtgaccaa gaaggagtac 300 ggccaggacc tgcaattcac cgccgaggtc gacatccgcc cgaagatcag tcccccggac 360 ctgagcgcgc tgacggtctc ggtggatccg atcgaaatcg gtgaggacga cgtcgacgcc 420 gaactgcagt cgttacgtac ccggttcggc accctgaccg cggtggaccg gccggtggcc 480 gtcggcgacg tcgtctcgat cgacttgtct gccacggtcg acggagagga cataccgaac 540 gcagccgctg agggactctc ccacgaggtc ggctccggcc ggctcatcgc aggtctcgac 600 gacgcggttg ttggtctgtc cgccgacgag tcccgggtct tcaccgccaa gctggcagcc 660 ggcgagcacg ccgggcagga agctcaggtt accgtcacgg tcaggtcggt taaggagcgc 720 gaactaccag agcccgacga cgaattcgcg cagttagcca gcgagttcga cagcatcgac 780 gaattgcggg ccagcctcag cgaccaggtg cgccaggcca agcgcgccca gcaggccgag 840 cagattcgaa acgccaccat cgatgcgcta ctcgaacagg tcgacgtgcc gttgccggag 900 tcgtatgtgc aggcccaatt cgacagcgtg ctgcacagcg cgctcagcgg tcttaatcac 960 gacgaagccc ggttcaatga gttgctcgtc gagcaaggct cgtcacgcgc ggcgttcgat 1020 gccgaggcgc gcaccgcctc agaaaaggac gtcaagaggc agctgttgct agacgccctg 1080 gccgatgagc tgcaggtcca agttggccag gatgatctga ccgaacgact ggtgacgacg 1140 tctcggcaat acggcatcga gccgcagcag ctgttcggct acctccaaga gcgcaaccag 1200 ctgccgacca tgttcgctga cgtgcggcgc gagctggcga tcagggccgc agtggaggcg 1260 gcgacggtca ccgacagtga cggaaacacg atcgatacca gtgagttctt cggcaagcgt 1320 gtgtcggccg gtgaggctga ggaggccgaa ccggcagacg agggtgccgc gcgggcggcg 1380 tccgacgaag cgacaacg 1398 57 313 DNA Mycobacterium tuberculosis 57 ccagagtgat tcgcctcggc tgggggccgg ctggccaggc atgtcgtcgt gtccgggggt 60 gccgtccatg cccgcagcgt atgtccaatt ggcgacgccg tcgggcaggc gcgcctggtt 120 cgaacgccgg ccgagcaccg agctggacgc ttgcggctgt acccgacacg cccggcgtgc 180 cggacgcgac gaaggtcact ttgactcgat attccctgga cagcgcaggt aacggtatgg 240 tttctaagcc aaagctcaga ttgctcatat atggcccata cgccggtacg cgacggtaat 300 tcccatggaa ctc 313 58 257 PRT Mycobacterium tuberculosis 58 Met Glu Leu Leu Gly Gly Pro Arg Val Gly Asn Thr Glu Ser Gln Leu 1 5 10 15 Cys Val Ala Asp Gly Asp Asp Leu Pro Thr Tyr Cys Ser Ala Asn Ser 20 25 30 Glu Asp Leu Asn Ile Thr Thr Ile Thr Thr Leu Ser Pro Thr Ser Met 35 40 45 Ser His Pro Gln Gln Val Arg Asp Asp Gln Trp Val Glu Pro Ser Asp 50 55 60 Gln Leu Gln Gly Thr Ala Val Phe Asp Ala Thr Gly Asp Lys Ala Thr 65 70 75 80 Met Pro Ser Trp Asp Glu Leu Val Arg Gln His Ala Asp Arg Val Tyr 85 90 95 Arg Leu Ala Tyr Arg Leu Ser Gly Asn Gln His Asp Ala Glu Asp Leu 100 105 110 Thr Gln Glu Thr Phe Ile Arg Val Phe Arg Ser Val Gln Asn Tyr Gln 115 120 125 Pro Gly Thr Phe Glu Gly Trp Leu His Arg Ile Thr Thr Asn Leu Phe 130 135 140 Leu Asp Met Val Arg Arg Arg Ala Arg Ile Arg Met Glu Ala Leu Pro 145 150 155 160 Glu Asp Tyr Asp Arg Val Pro Ala Asp Glu Pro Asn Pro Glu Gln Ile 165 170 175 Tyr His Asp Ala Arg Leu Gly Pro Asp Leu Gln Ala Ala Leu Ala Ser 180 185 190 Leu Pro Pro Glu Phe Arg Ala Ala Val Val Leu Cys Asp Ile Glu Gly 195 200 205 Leu Ser Tyr Glu Glu Ile Gly Ala Thr Leu Gly Val Lys Leu Gly Thr 210 215 220 Val Arg Ser Arg Ile His Arg Gly Arg Gln Ala Leu Arg Asp Tyr Leu 225 230 235 240 Ala Ala His Pro Glu His Gly Glu Cys Ala Val His Val Asn Pro Val 245 250 255 Arg 59 771 DNA Mycobacterium tuberculosis 59 atggaactcc tcggcggacc ccgggttggg aatacggaat cgcaactttg cgttgccgac 60 ggtgacgact tgccaactta ttgcagtgca aattcggagg atctcaatat cacgaccatc 120 acgaccttga gtccgaccag catgtctcat ccccaacagg tccgcgatga ccagtgggtg 180 gagccgtctg accaattgca gggcaccgcc gtattcgacg ccaccgggga caaggccacc 240 atgccgtcct gggatgagct ggtccgtcag cacgccgatc gggtgtaccg gctggcttat 300 cggctctccg gcaaccagca cgatgccgaa gacctgaccc aggagacctt tatcagggtg 360 ttccggtcgg tccagaatta ccagccgggc accttcgaag gctggctaca ccgcatcacc 420 accaacttgt tcctggacat ggtccgccgc cgggctcgca tccggatgga ggcgttaccc 480 gaggactacg accgggtgcc cgccgatgag cccaaccccg agcagatcta ccacgacgca 540 cggctgggac ctgacctgca ggctgccttg gcctcgctgc cgccggagtt tcgtgccgcg 600 gtggtgctgt gtgacatcga gggtctgtcg tacgaggaga tcggcgccac actgggcgtg 660 aagctcggga cggtacgtag ccggatacac cgcggacgcc aggcactgcg ggactacctg 720 gcagcgcacc ccgaacatgg cgagtgcgca gttcacgtca acccagttcg c 771 60 154 PRT Mycobacterium tuberculosis 60 Met Ala Asp Pro Gly Ser Val Gly His Val Phe Arg Arg Ala Phe Ser 1 5 10 15 Trp Leu Pro Ala Gln Phe Ala Ser Gln Ser Asp Ala Pro Val Gly Ala 20 25 30 Pro Arg Gln Phe Arg Ser Thr Glu His Leu Ser Ile Glu Ala Ile Ala 35 40 45 Ala Phe Val Asp Gly Glu Leu Arg Met Asn Ala His Leu Arg Ala Ala 50 55 60 His His Leu Ser Leu Cys Ala Gln Cys Ala Ala Glu Val Asp Asp Gln 65 70 75 80 Ser Arg Ala Arg Ala Ala Leu Arg Asp Ser His Pro Ile Arg Ile Pro 85 90 95 Ser Thr Leu Leu Gly Leu Leu Ser Glu Ile Pro Arg Cys Pro Pro Glu 100 105 110 Gly Pro Ser Lys Gly Ser Ser Gly Gly Ser Ser Gln Gly Pro Pro Asp 115 120 125 Gly Ala Ala Ala Gly Phe Gly Asp Arg Phe Ala Asp Gly Asp Gly Gly 130 135 140 Asn Arg Gly Arg Gln Ser Arg Val Arg Arg 145 150 61 462 DNA Mycobacterium tuberculosis 61 atggccgacc ccggaagcgt gggacatgtg ttccggcgcg cgttttcctg gctcccggcg 60 cagttcgcct cccagagtga cgcgccggtc ggcgcgccgc ggcagttccg ttccaccgag 120 cacctgtcaa tcgaggccat cgcggctttc gtcgacggcg agctgcggat gaacgcgcac 180 ttgcgggccg cgcatcacct ttcgctgtgt gcccaatgcg cggccgaagt ggacgaccaa 240 agtcgtgccc gcgccgctct gcgcgattcc cacccgatcc gcatccccag cacgttgctc 300 ggattactgt ccgagatccc gcgttgtcca cctgaaggtc catctaaagg ttcgtctgga 360 ggttcatccc agggcccgcc cgacggggct gcggcaggct tcggcgaccg cttcgctgac 420 ggcgatggcg ggaatcgggg ccggcaatcg cgggtgcgtc gc 462 62 549 PRT Mycobacterium tuberculosis 62 Val Ser His Leu Ser Gln Arg Met Ala Gly Leu Leu Arg Val His Gly 1 5 10 15 Glu Trp Ser Arg Ser Val Asp Thr Arg Val Asp Thr Asp Asn Ala Met 20 25 30 Pro Ala Arg Phe Ser Ala Gln Ile Gln Asn Glu Asp Glu Val Thr Ser 35 40 45 Asp Gln Gly Asn Asn Gly Gly Pro Asn Gly Gly Gly Arg Leu Ala Pro 50 55 60 Arg Pro Val Phe Arg Pro Pro Val Asp Pro Ala Ser Arg Gln Ala Phe 65 70 75 80 Gly Arg Pro Ser Gly Val Gln Gly Ser Phe Val Ala Glu Arg Val Arg 85 90 95 Pro Gln Lys Tyr Gln Asp Gln Ser Asp Phe Thr Pro Asn Asp Gln Leu 100 105 110 Ala Asp Pro Val Leu Gln Glu Ala Phe Gly Arg Pro Phe Ala Gly Ala 115 120 125 Glu Ser Leu Gln Arg His Pro Ile Asp Ala Gly Ala Leu Ala Ala Glu 130 135 140 Lys Asp Gly Ala Gly Pro Asp Glu Pro Asp Asp Pro Trp Arg Asp Pro 145 150 155 160 Ala Ala Ala Ala Ala Leu Gly Thr Pro Ala Leu Ala Ala Pro Ala Pro 165 170 175 His Gly Ala Leu Ala Gly Ser Gly Lys Leu Gly Val Arg Asp Val Leu 180 185 190 Phe Gly Gly Lys Val Ser Tyr Leu Ala Leu Gly Ile Leu Val Ala Ile 195 200 205 Ala Leu Val Ile Gly Gly Ile Gly Gly Val Ile Gly Arg Lys Thr Ala 210 215 220 Glu Val Val Asp Ala Phe Thr Thr Ser Lys Val Thr Leu Ser Thr Thr 225 230 235 240 Gly Asn Ala Gln Glu Pro Ala Gly Arg Phe Thr Lys Val Ala Ala Ala 245 250 255 Val Ala Asp Ser Val Val Thr Ile Glu Ser Val Ser Asp Gln Glu Gly 260 265 270 Met Gln Gly Ser Gly Val Ile Val Asp Gly Arg Gly Tyr Ile Val Thr 275 280 285 Asn Asn His Val Ile Ser Glu Ala Ala Asn Asn Pro Ser Gln Phe Lys 290 295 300 Thr Thr Val Val Phe Asn Asp Gly Lys Glu Val Pro Ala Asn Leu Val 305 310 315 320 Gly Arg Asp Pro Lys Thr Asp Leu Ala Val Leu Lys Val Asp Asn Val 325 330 335 Asp Asn Leu Thr Val Ala Arg Leu Gly Asp Ser Ser Lys Val Arg Val 340 345 350 Gly Asp Glu Val Leu Ala Val Gly Ala Pro Leu Gly Leu Arg Ser Thr 355 360 365 Val Thr Gln Gly Ile Val Ser Ala Leu His Arg Pro Val Pro Leu Ser 370 375 380 Gly Glu Gly Ser Asp Thr Asp Thr Val Ile Asp Ala Ile Gln Thr Asp 385 390 395 400 Ala Ser Ile Asn His Gly Asn Ser Gly Gly Pro Leu Ile Asp Met Asp 405 410 415 Ala Gln Val Ile Gly Ile Asn Thr Ala Gly Lys Ser Leu Ser Asp Ser 420 425 430 Ala Ser Gly Leu Gly Phe Ala Ile Pro Val Asn Glu Met Lys Leu Val 435 440 445 Ala Asn Ser Leu Ile Lys Asp Gly Lys Ile Val His Pro Thr Leu Gly 450 455 460 Ile Ser Thr Arg Ser Val Ser Asn Ala Ile Ala Ser Gly Ala Gln Val 465 470 475 480 Ala Asn Val Lys Ala Gly Ser Pro Ala Gln Lys Gly Gly Ile Leu Glu 485 490 495 Asn Asp Val Ile Val Lys Val Gly Asn Arg Ala Val Ala Asp Ser Asp 500 505 510 Glu Phe Val Val Ala Val Arg Gln Leu Ala Ile Gly Gln Asp Ala Pro 515 520 525 Ile Glu Val Val Arg Glu Gly Arg His Val Thr Leu Thr Val Lys Pro 530 535 540 Asp Pro Asp Ser Thr 545 63 1647 DNA Mycobacterium tuberculosis 63 gtgagccact tgtcgcagcg catggcgggg ttgctgcgag ttcatggcga gtggtcgcga 60 tccgtggata ctagggtgga cacggacaac gcgatgcctg cacgttttag cgcccagatt 120 cagaatgagg atgaggtgac ctccgaccaa ggcaacaacg gcggcccgaa cggcggaggc 180 cgcctggcgc cgcgcccggt ttttcggcca ccggtcgacc cggcgtcgcg tcaagcgttc 240 gggcgtccgt ccggggtcca agggtccttt gtggccgagc gtgtgcgccc gcagaagtac 300 caggaccagt ctgacttcac accgaacgat cagcttgctg acccggtgct tcaggaggcg 360 ttcggtcgtc cgttcgcggg cgccgaatcg ctgcagcgcc atcccatcga tgccggagcg 420 ctggcagctg agaaagacgg tgccggcccc gacgagcccg acgatccgtg gcgcgacccc 480 gcggccgcgg ccgcgctggg gacgccagcg ctagccgcgc cggcaccgca cggtgcgctg 540 gccggcagcg gcaagctggg tgtgcgcgac gtgctgtttg gcggcaaggt gtcctacttg 600 gcgctgggca tcttggtcgc tatcgcactg gtgatcggcg gcatcggcgg tgtcatcggc 660 cgcaagaccg cggaagtagt cgatgcgttc accacgtcga aggtgaccct gtcgaccact 720 ggcaatgccc aggaaccggc cggccggttc accaaggtgg cggccgccgt ggccgattcg 780 gtggtgacca ttgagtcggt cagcgaccag gagggcatgc aaggttccgg cgtcatcgtc 840 gatggccgcg gctacatcgt caccaacaat cacgtgatct ctgaggcggc caacaatccc 900 agccagttca agacgaccgt ggtgttcaac gacggcaagg aggtgcccgc caatctggtg 960 ggtcgtgacc ccaagaccga cttggccgtc ctcaaggtcg acaacgtcga caatctgacc 1020 gtggcccggc tcggtgattc cagcaaggta cgggtcggtg acgaagtcct cgcggtcggc 1080 gcgcccctgg ggctgcgcag tacggtgacc cagggcattg tcagcgcgct acaccgcccc 1140 gttccgttgt cgggcgaggg ctctgacacc gacaccgtca ttgacgcaat tcagaccgac 1200 gcctcgatca accacggtaa ctccggcggt ccgctaatcg acatggatgc ccaggtgatt 1260 ggcatcaaca ccgccggtaa gtcactgtcg gatagcgcca gcgggctggg ctttgcgatc 1320 ccggtcaacg agatgaaatt ggtggcaaat tctctgatca aagacggaaa gatcgtgcat 1380 ccgacgttgg gcatcagcac ccggtcagta agcaacgcga tcgcgtcggg cgcgcaggtg 1440 gccaatgtaa aggcgggaag tcccgcgcag aagggcggga tcttggagaa cgatgtgatc 1500 gtcaaggtcg gtaaccgcgc ggtcgccgac tccgacgagt tcgtcgtcgc cgtgcgccag 1560 ttggctatcg gccaggacgc tccgatagag gtggtccgcg agggtcggca tgtgacgctg 1620 acggtgaaac cggaccccga tagcacc 1647 64 131 PRT Mycobacterium tuberculosis 64 Val Phe Ala Asn Ile Gly Trp Trp Glu Met Leu Val Leu Val Met Val 1 5 10 15 Gly Leu Val Val Leu Gly Pro Glu Arg Leu Pro Gly Ala Ile Arg Trp 20 25 30 Ala Ala Ser Ala Leu Arg Gln Ala Arg Asp Tyr Leu Ser Gly Val Thr 35 40 45 Ser Gln Leu Arg Glu Asp Ile Gly Pro Glu Phe Asp Asp Leu Arg Gly 50 55 60 His Leu Gly Glu Leu Gln Lys Leu Arg Gly Met Thr Pro Arg Ala Ala 65 70 75 80 Leu Thr Lys His Leu Leu Asp Gly Asp Asp Ser Leu Phe Thr Gly Asp 85 90 95 Phe Asp Arg Pro Thr Pro Lys Lys Pro Asp Ala Ala Gly Ser Ala Gly 100 105 110 Pro Asp Ala Thr Glu Gln Ile Gly Ala Gly Pro Ile Pro Phe Asp Ser 115 120 125 Asp Ala Thr 130 65 393 DNA Mycobacterium tuberculosis 65 gtgttcgcca acatcggttg gtgggaaatg ctcgtcctcg tcatggtcgg gctggtggtg 60 cttggcccgg agcggctccc gggtgccatc cgctgggcgg caagcgctct gcggcaggcg 120 cgcgactatc tcagcggtgt gaccagccag ctacgtgagg acattggacc cgaattcgat 180 gatctgcggg gacatctcgg tgagctgcag aagctacggg gaatgactcc gcgggctgcg 240 ttgaccaagc acctactgga tggcgatgat tccctgttca ccggagactt cgaccgaccg 300 acgccgaaga aaccggatgc ggcgggctcg gcggggccgg acgctactga gcagatcggt 360 gcggggccca tcccgtttga cagcgatgcc acc 393 66 185 DNA Mycobacterium tuberculosis 66 gccagccaca tctatctctt ctcgtgttgc cgcgctaacc gggcggttgt ttgcggcaaa 60 cgcgcgaggt caccgttggg tcacattagt cgcacgtacc gggggcagtt tgtgacttac 120 gtttccatag cgtcagatgt gacgtacggt gcaaatgatg cttgtggtgt cgttggcgtt 180 gacct 185 67 472 PRT Mycobacterium tuberculosis 67 Met Arg Arg Asn Arg Arg Gly Ser Pro Ala Arg Pro Ala Ala Arg Phe 1 5 10 15 Val Arg Pro Ala Ile Pro Ser Ala Leu Ser Val Ala Leu Leu Val Cys 20 25 30 Thr Pro Gly Leu Ala Thr Ala Asp Pro Gln Thr Asp Thr Ile Ala Ala 35 40 45 Leu Ile Ala Asp Val Ala Lys Ala Asn Gln Arg Leu Gln Asp Leu Ser 50 55 60 Asp Glu Val Gln Ala Glu Gln Glu Ser Val Asn Lys Ala Met Val Asp 65 70 75 80 Val Glu Thr Ala Arg Asp Asn Ala Ala Ala Ala Glu Asp Asp Leu Glu 85 90 95 Val Ser Gln Arg Ala Val Lys Asp Ala Asn Ala Ala Ile Ala Ala Ala 100 105 110 Gln His Arg Phe Asp Thr Phe Ala Ala Ala Thr Tyr Met Asn Gly Pro 115 120 125 Ser Val Ser Tyr Leu Ser Ala Ser Ser Pro Asp Glu Ile Ile Ala Thr 130 135 140 Val Thr Ala Ala Lys Thr Leu Ser Ala Ser Ser Gln Ala Val Met Ala 145 150 155 160 Asn Leu Gln Arg Ala Arg Thr Glu Arg Val Asn Thr Glu Ser Ala Ala 165 170 175 Arg Leu Ala Lys Gln Lys Ala Asp Lys Ala Ala Ala Asp Ala Lys Ala 180 185 190 Ser Gln Asp Ala Ala Val Ala Ala Leu Thr Glu Thr Arg Arg Lys Phe 195 200 205 Asp Glu Gln Arg Glu Glu Val Gln Arg Leu Ala Ala Glu Arg Asp Ala 210 215 220 Ala Gln Ala Arg Leu Gln Ala Ala Arg Leu Val Ala Trp Ser Ser Glu 225 230 235 240 Gly Gly Gln Gly Ala Pro Pro Phe Arg Met Trp Asp Pro Gly Ser Gly 245 250 255 Pro Ala Gly Gly Arg Ala Trp Asp Gly Leu Trp Asp Pro Thr Leu Pro 260 265 270 Met Ile Pro Ser Ala Asn Ile Pro Gly Asp Pro Ile Ala Val Val Asn 275 280 285 Gln Val Leu Gly Ile Ser Ala Thr Ser Ala Gln Val Thr Ala Asn Met 290 295 300 Gly Arg Lys Phe Leu Glu Gln Leu Gly Ile Leu Gln Pro Thr Asp Thr 305 310 315 320 Gly Ile Thr Asn Ala Pro Ala Gly Ser Ala Gln Gly Arg Ile Pro Arg 325 330 335 Val Tyr Gly Arg Gln Ala Ser Glu Tyr Val Ile Arg Arg Gly Met Ser 340 345 350 Gln Ile Gly Val Pro Tyr Ser Trp Gly Gly Gly Asn Ala Ala Gly Pro 355 360 365 Ser Lys Gly Ile Asp Ser Gly Ala Gly Thr Val Gly Phe Asp Cys Ser 370 375 380 Gly Leu Val Leu Tyr Ser Phe Ala Gly Val Gly Ile Lys Leu Pro His 385 390 395 400 Tyr Ser Gly Ser Gln Tyr Asn Leu Gly Arg Lys Ile Pro Ser Ser Gln 405 410 415 Met Arg Arg Gly Asp Val Ile Phe Tyr Gly Pro Asn Gly Ser Gln His 420 425 430 Val Thr Ile Tyr Leu Gly Asn Gly Gln Met Leu Glu Ala Pro Asp Val 435 440 445 Gly Leu Lys Val Arg Val Ala Pro Val Arg Thr Ala Gly Met Thr Pro 450 455 460 Tyr Val Val Arg Tyr Ile Glu Tyr 465 470 68 1416 DNA Mycobacterium tuberculosis 68 atgagacgga atcgccgtgg ctcgccagcg cgaccggccg cacggtttgt ccgtccggca 60 attccgtcgg ctttgagtgt ggccctgctg gtatgcacac cggggctggc taccgccgat 120 ccacagacgg acaccatcgc cgcgctgatt gccgacgtcg ccaaggccaa ccagcgcctg 180 caagacctga gcgacgaggt tcaggccgaa caggaaagcg ttaacaaggc gatggtcgac 240 gtggaaaccg ctcgggacaa cgctgccgcg gccgaagacg acctggaggt cagccagcgc 300 gcggttaagg acgccaacgc ggcgatcgcc gcggctcagc accggttcga caccttcgcg 360 gcggccacct acatgaacgg tccctcggtc agctacctca gcgcgagcag ccccgacgag 420 atcattgcca ctgtgaccgc cgccaagacc cttagcgcca gttcccaagc ggtgatggcc 480 aacctgcagc gggcccggac cgagcgggtg aacacggagt cggcggcgcg gctagccaag 540 cagaaggctg ataaggccgc cgccgacgca aaggccagcc aggatgccgc ggtggcggcg 600 ctcaccgaga cccggcggaa gttcgatgaa cagcgcgagg aggtccaacg cctggccgcc 660 gagcgcgatg cggctcaagc ccgactgcag gcggccaggt tggttgcctg gtcctcggag 720 ggtggtcagg gtgcgccgcc gttccggatg tgggatcccg gatcgggccc tgccggtggg 780 cgtgcatggg atggcttgtg ggaccccacg ctgcccatga tccccagcgc caacatcccc 840 ggcgacccga tcgcggtagt gaaccaggtg ttggggatct cggcaacgtc agcgcaggtc 900 accgccaata tggggcgcaa gttcctggag cagctgggca tcttgcagcc caccgatacc 960 ggcatcacca acgctccggc gggctcggcc cagggccgga ttccgcgagt ttatgggcgc 1020 caggcttctg aatacgtgat ccgccgcggc atgtcacaga tcggggtgcc ctattcctgg 1080 ggcggcggca atgccgcggg cccgagcaag ggcatcgact ccggggccgg caccgtcggc 1140 ttcgactgct caggcctggt gttgtactcg tttgctgggg tgggcatcaa gctgccgcac 1200 tactcgggtt cgcagtacaa cctgggccgc aagatcccgt cctcgcagat gcgccgcggc 1260 gacgtcatct tctacggccc gaacggtagc cagcacgtga cgatctacct cggcaacggc 1320 cagatgctcg aggcgcccga cgtcggtttg aaggtgcggg ttgcgcccgt gcgcacggct 1380 ggcatgaccc cgtatgtggt ccgatacatc gagtac 1416 69 241 PRT Mycobacterium tuberculosis 69 Met Arg His Thr Arg Phe His Pro Ile Lys Leu Ala Trp Ile Thr Ala 1 5 10 15 Val Val Ala Gly Leu Met Val Gly Val Ala Thr Pro Ala Asp Ala Glu 20 25 30 Pro Gly Gln Trp Asp Pro Thr Leu Pro Ala Leu Val Ser Ala Gly Ala 35 40 45 Pro Gly Asp Pro Leu Ala Val Ala Asn Ala Ser Leu Gln Ala Thr Ala 50 55 60 Gln Ala Thr Gln Thr Thr Leu Asp Leu Gly Arg Gln Phe Leu Gly Gly 65 70 75 80 Leu Gly Ile Asn Leu Gly Gly Pro Ala Ala Ser Ala Pro Ser Ala Ala 85 90 95 Thr Thr Gly Ala Ser Arg Ile Pro Arg Ala Asn Ala Arg Gln Ala Val 100 105 110 Glu Tyr Val Ile Arg Arg Ala Gly Ser Gln Met Gly Val Pro Tyr Ser 115 120 125 Trp Gly Gly Gly Ser Leu Gln Gly Pro Ser Lys Gly Val Asp Ser Gly 130 135 140 Ala Asn Thr Val Gly Phe Asp Cys Ser Gly Leu Val Arg Tyr Ala Phe 145 150 155 160 Ala Gly Val Gly Val Leu Ile Pro Arg Phe Ser Gly Asp Gln Tyr Asn 165 170 175 Ala Gly Arg His Val Pro Pro Ala Glu Ala Lys Arg Gly Asp Leu Ile 180 185 190 Phe Tyr Gly Pro Gly Gly Gly Gln His Val Thr Leu Tyr Leu Gly Asn 195 200 205 Gly Gln Met Leu Glu Ala Ser Gly Ser Ala Gly Lys Val Thr Val Ser 210 215 220 Pro Val Arg Lys Ala Gly Met Thr Pro Phe Val Thr Arg Ile Ile Glu 225 230 235 240 Tyr 70 723 DNA Mycobacterium tuberculosis 70 atgcgccaca cgcgttttca cccgatcaaa ctggcctgga tcaccgcggt ggttgccggc 60 ctgatggtcg gtgtggcaac gcccgccgat gccgaacccg gacaatggga tcccacgctg 120 ccggcattgg tcagtgcggg ggcgcccgga gatccgctgg cggtagccaa cgcgtcgttg 180 caggccaccg cccaggccac ccagaccacg ctggatttgg gcaggcagtt cctcggtggg 240 ttgggaatca acctcggcgg ccctgctgcc agcgctccca gcgccgccac aaccggcgcg 300 agccggattc cgcgggccaa cgcccgtcag gccgtcgaat atgtgattcg ccgggccggg 360 tcgcagatgg gggtgcccta ttcgtggggt ggtggctcgc ttcagggccc cagcaagggc 420 gtggactcgg gggccaacac tgtcggcttc gactgctcag gtctggtgcg gtatgccttc 480 gccggggtcg gcgtgctgat cccgcggttc tccggtgatc agtacaacgc cggtcgccac 540 gttccgcccg ctgaggccaa gcgcggcgac ctgatctttt acggcccagg cggcggccag 600 cacgtcaccc tgtatctggg caacggccaa atgctggagg catccggaag cgccggcaaa 660 gtcacggtga gcccggtgcg aaaggccgga atgacgccgt tcgtgactag gatcatcgaa 720 tac 723 71 180 DNA Mycobacterium tuberculosis 71 ggacacctcg tgattatgcg cctgctgcgg ccagcgcggg aacaccttgg ctggtccact 60 acggccggca cggacggctg cgcggtaggg tacgcggcag caccatatcg ggccgcttca 120 gttgtcgttt cgggagtcgc gcatgtcggg tcggaaattt tcgttcgagg tcaccaagac 180 72 154 PRT Mycobacterium tuberculosis 72 Met Ser Gly Arg Lys Phe Ser Phe Glu Val Thr Lys Thr Ser Ser Ala 1 5 10 15 Pro Ala Ala Thr Leu Phe Arg Leu Val Thr Asp Gly Gly Asn Trp Ala 20 25 30 Thr Trp Ala Lys Pro Ile Val Ala Gln Ser Ser Trp Ala Arg Arg Gly 35 40 45 Asp Pro Ala Pro Gly Gly Ile Gly Ala Ile Arg Lys Leu Gly Met Trp 50 55 60 Pro Val Phe Val Gln Glu Glu Thr Val Glu Tyr Glu Gln Asp Arg Arg 65 70 75 80 His Val Tyr Lys Leu Val Gly Ala Arg Thr Pro Val Gln Asp Tyr Phe 85 90 95 Gly Glu Val Val Leu Thr Pro Asn Ala Ser Gly Gly Thr Asp Leu Arg 100 105 110 Trp Ser Gly Ser Phe Thr Glu Lys Val Arg Gly Thr Gly Pro Val Met 115 120 125 Arg Ala Ala Leu Gly Gly Ala Val Arg Phe Phe Ala Gly Gln Leu Val 130 135 140 Lys Ala Ala Glu Arg Glu Ala Val Arg Arg 145 150 73 462 DNA Mycobacterium tuberculosis 73 atgtcgggtc ggaaattttc gttcgaggtc accaagacca gcagcgcgcc ggctgcaacc 60 ttgtttcggc tcgtgacaga cggtggcaac tgggcgacct gggccaagcc catcgttgct 120 caatcgagtt gggcgcgacg cggtgatccc gcgcccggcg gcatcggggc catccgcaaa 180 ctaggcatgt ggccggtgtt cgtgcaggaa gagaccgtcg agtatgagca ggaccgtcgc 240 cacgtctaca agctggttgg cgcgaggaca cccgtccagg actacttcgg cgaggtggtc 300 cttacaccaa atgcgtcggg cggtaccgat ctccgctgga gtggctcgtt taccgaaaag 360 gttcgtggga cggggccggt gatgcgggcg gcgctgggtg gcgcggtcag gttcttcgcg 420 ggtcaactgg tgaaggcggc cgagcgggag gcggtgcgcc gg 462 74 140 DNA Mycobacterium tuberculosis 74 cacggacctc gattctaagc tcgcggcgaa acggcggcgg atgcacaagt gggtaaaatt 60 gagcggaaca gactcaacat tgacggcgtt gaacaacccg acaagcattt cgaacggacc 120 ccgaatggag gtgtcgtgga 140 75 848 PRT Mycobacterium tuberculosis 75 Val Asp Ser Phe Asn Pro Thr Thr Lys Thr Gln Ala Ala Leu Thr Ala 1 5 10 15 Ala Leu Gln Ala Ala Ser Thr Ala Gly Asn Pro Glu Ile Arg Pro Ala 20 25 30 His Leu Leu Met Ala Leu Leu Thr Gln Asn Asp Gly Ile Ala Ala Pro 35 40 45 Leu Leu Glu Ala Val Gly Val Glu Pro Ala Thr Val Arg Ala Glu Thr 50 55 60 Gln Arg Leu Leu Asp Arg Leu Pro Gln Ala Thr Gly Ala Ser Thr Gln 65 70 75 80 Pro Gln Leu Ser Arg Glu Ser Leu Ala Ala Ile Thr Thr Ala Gln Gln 85 90 95 Leu Ala Thr Glu Leu Asp Asp Glu Tyr Val Ser Thr Glu His Val Met 100 105 110 Val Gly Leu Ala Thr Gly Asp Ser Asp Val Ala Lys Leu Leu Thr Gly 115 120 125 His Gly Ala Ser Pro Gln Ala Leu Arg Glu Ala Phe Val Lys Val Arg 130 135 140 Gly Ser Ala Arg Val Thr Ser Pro Glu Pro Glu Ala Thr Tyr Gln Ala 145 150 155 160 Leu Gln Lys Tyr Ser Thr Asp Leu Thr Ala Arg Ala Arg Glu Gly Lys 165 170 175 Leu Asp Pro Val Ile Gly Arg Asp Asn Glu Ile Arg Arg Val Val Gln 180 185 190 Val Leu Ser Arg Arg Thr Lys Asn Asn Pro Val Leu Ile Gly Glu Pro 195 200 205 Gly Val Gly Lys Thr Ala Ile Val Glu Gly Leu Ala Gln Arg Ile Val 210 215 220 Ala Gly Asp Val Pro Glu Ser Leu Arg Asp Lys Thr Ile Val Ala Leu 225 230 235 240 Asp Leu Gly Ser Met Val Ala Gly Ser Lys Tyr Arg Gly Glu Phe Glu 245 250 255 Glu Arg Leu Lys Ala Val Leu Asp Asp Ile Lys Asn Ser Ala Gly Gln 260 265 270 Ile Ile Thr Phe Ile Asp Glu Leu His Thr Ile Val Gly Ala Gly Ala 275 280 285 Thr Gly Glu Gly Ala Met Asp Ala Gly Asn Met Ile Lys Pro Met Leu 290 295 300 Ala Arg Gly Glu Leu Arg Leu Val Gly Ala Thr Thr Leu Asp Glu Tyr 305 310 315 320 Arg Lys His Ile Glu Lys Asp Ala Ala Leu Glu Arg Arg Phe Gln Gln 325 330 335 Val Tyr Val Gly Glu Pro Ser Val Glu Asp Thr Ile Gly Ile Leu Arg 340 345 350 Gly Leu Lys Asp Arg Tyr Glu Val His His Gly Val Arg Ile Thr Asp 355 360 365 Ser Ala Leu Val Ala Ala Ala Thr Leu Ser Asp Arg Tyr Ile Thr Ala 370 375 380 Arg Phe Leu Pro Asp Lys Ala Ile Asp Leu Val Asp Glu Ala Ala Ser 385 390 395 400 Arg Leu Arg Met Glu Ile Asp Ser Arg Pro Val Glu Ile Asp Glu Val 405 410 415 Glu Arg Leu Val Arg Arg Leu Glu Ile Glu Glu Met Ala Leu Ser Lys 420 425 430 Glu Glu Asp Glu Ala Ser Ala Glu Arg Leu Ala Lys Leu Arg Ser Glu 435 440 445 Leu Ala Asp Gln Lys Glu Lys Leu Ala Glu Leu Thr Thr Arg Trp Gln 450 455 460 Asn Glu Lys Asn Ala Ile Glu Ile Val Arg Asp Leu Lys Glu Gln Leu 465 470 475 480 Glu Ala Leu Arg Gly Glu Ser Glu Arg Ala Glu Arg Asp Gly Asp Leu 485 490 495 Ala Lys Ala Ala Glu Leu Arg Tyr Gly Arg Ile Pro Glu Val Glu Lys 500 505 510 Lys Leu Asp Ala Ala Leu Pro Gln Ala Gln Ala Arg Glu Gln Val Met 515 520 525 Leu Lys Glu Glu Val Gly Pro Asp Asp Ile Ala Asp Val Val Ser Ala 530 535 540 Trp Thr Gly Ile Pro Ala Gly Arg Leu Leu Glu Gly Glu Thr Ala Lys 545 550 555 560 Leu Leu Arg Met Glu Asp Glu Leu Gly Lys Arg Val Ile Gly Gln Lys 565 570 575 Ala Ala Val Thr Ala Val Ser Asp Ala Val Arg Arg Ser Arg Ala Gly 580 585 590 Val Ser Asp Pro Asn Arg Pro Thr Gly Ala Phe Met Phe Leu Gly Pro 595 600 605 Thr Gly Val Gly Lys Thr Glu Leu Ala Lys Ala Leu Ala Asp Phe Leu 610 615 620 Phe Asp Asp Glu Arg Ala Met Val Arg Ile Asp Met Ser Glu Tyr Gly 625 630 635 640 Glu Lys His Thr Val Ala Arg Leu Ile Gly Ala Pro Pro Gly Tyr Val 645 650 655 Gly Tyr Glu Ala Gly Gly Gln Leu Thr Glu Ala Val Arg Arg Arg Pro 660 665 670 Tyr Thr Val Val Leu Phe Asp Glu Ile Glu Lys Ala His Pro Asp Val 675 680 685 Phe Asp Val Leu Leu Gln Val Leu Asp Glu Gly Arg Leu Thr Asp Gly 690 695 700 His Gly Arg Thr Val Asp Phe Arg Asn Thr Ile Leu Ile Leu Thr Ser 705 710 715 720 Asn Leu Gly Ser Gly Gly Ser Ala Glu Gln Val Leu Ala Ala Val Arg 725 730 735 Ala Thr Phe Lys Pro Glu Phe Ile Asn Arg Leu Asp Asp Val Leu Ile 740 745 750 Phe Glu Gly Leu Asn Pro Glu Glu Leu Val Arg Ile Val Asp Ile Gln 755 760 765 Leu Ala Gln Leu Gly Lys Arg Leu Ala Gln Arg Arg Leu Gln Leu Gln 770 775 780 Val Ser Leu Pro Ala Lys Arg Trp Leu Ala Gln Arg Gly Phe Asp Pro 785 790 795 800 Val Tyr Gly Ala Arg Pro Leu Arg Arg Leu Val Gln Gln Ala Ile Gly 805 810 815 Asp Gln Leu Ala Lys Met Leu Leu Ala Gly Gln Val His Asp Gly Asp 820 825 830 Thr Val Pro Val Asn Val Ser Pro Asp Ala Asp Ser Leu Ile Leu Gly 835 840 845 76 2544 DNA Mycobacterium tuberculosis 76 gtggactcgt ttaacccgac gaccaagacg caggcggcgc taaccgcggc gttacaggcg 60 gcttcgaccg ccggcaatcc cgagatccgg cccgctcacc tgctgatggc gctgctgacc 120 caaaacgacg gtatcgccgc accgctactg gaggctgtcg gtgtcgagcc cgccaccgtc 180 cgcgccgaaa cccagcgcct gctcgaccgt ttgccgcagg cgactggagc cagcacgcag 240 ccgcagctgt cccgcgagtc gttagcggcg atcaccaccg cgcagcagct ggccaccgag 300 ctggacgacg agtacgtctc caccgagcac gtgatggtcg ggctggccac cggtgactcc 360 gacgtcgcca agctgttgac cggccacggc gcctcgccgc aggcgctgcg ggaggcgttc 420 gtcaaggtgc gcggcagcgc ccgggtcacc agccccgaac cggaggcgac ctatcaggcg 480 ctgcagaagt actccaccga cctgaccgcc cgcgcccgcg aaggcaaact cgacccggtc 540 atcggccgcg acaacgagat ccgccgcgtg gtgcaggtgc tgtcccgtcg caccaagaac 600 aacccggtgc tgatcggtga gcccggcgtc ggcaagaccg cgatcgtgga gggcctggcg 660 cagcgcatcg tggccggcga cgtgccggag agcttgcgcg acaagaccat cgtcgcgctc 720 gatctcggct cgatggtcgc cggctccaaa taccgcggcg aattcgagga acggctcaag 780 gccgtcctcg acgacatcaa gaactcggcc ggccaaatca tcacgttcat cgacgagctg 840 cacaccatcg tcggcgccgg cgccaccggc gagggggcga tggacgccgg caacatgatc 900 aagccgatgc tggcccgcgg cgagttacgg ctggtcgggg cgaccacgct ggacgaatac 960 cgcaagcaca tcgagaagga cgccgcgctc gagcgccgtt tccaacaggt gtacgtcggc 1020 gagccgtcgg tggaggacac catcggcatc ctgcgcgggc tcaaagaccg ctacgaggtg 1080 caccacgggg tgcgcatcac cgactcggcg ctggtggcag ctgccacttt gagcgaccgg 1140 tatatcaccg cccgcttcct gcccgacaag gccatcgacc tggtcgacga ggcggccagc 1200 cggctgcgga tggagatcga ctcgcggccc gtcgagatcg acgaggtcga gcggctggtg 1260 cgccggctgg agatcgaaga gatggcgctg tccaaagaag aagacgaggc gtcggcggag 1320 cggttggcca agctgcgctc cgagctggcc gaccagaaag agaagttggc cgagctcacc 1380 acccgctggc agaacgagaa gaacgcgatc gaaatcgtcc gcgacctcaa ggagcagctg 1440 gaagccctgc gcggggaatc cgagcgggcc gaacgcgacg gcgacctggc caaggccgcc 1500 gagctgcgct acggacgcat ccccgaggtg gagaagaagc tcgacgcggc gttgccgcag 1560 gcgcaggccc gggagcaggt gatgctcaag gaggaggtcg gtcccgacga catcgccgac 1620 gtggtgtcgg cgtggaccgg catcccggcc ggtcggctgc tggaaggcga gaccgccaag 1680 ctgctgcgca tggaagacga gctgggcaag cgggtcatcg ggcagaaggc cgcggttacc 1740 gcagtctctg atgcggtgcg gcgcagccgg gccggggtgt ccgaccccaa ccggcccacc 1800 ggggcgttca tgttcctcgg cccgaccggt gtcggcaaga ccgagctggc caaggcgctg 1860 gccgacttcc tgttcgacga cgagcgggcg atggtccgca tcgacatgag cgagtacggc 1920 gagaagcaca ccgtggctcg gttgatcggc gccccgcccg gctatgtggg atacgaggcg 1980 ggcggtcagc tgaccgaggc ggtgcgccgg cgtccctaca cggtggtgct gttcgacgag 2040 atcgagaagg cgcacccgga cgtgttcgac gtgctgctgc aggtcctcga cgagggccgg 2100 ctcaccgacg ggcacggccg cacggtcgac ttccgcaaca ccatcttgat cctgacgtcc 2160 aacctggggt cgggtggcag cgccgagcag gtgctggccg cggtgcgcgc tacgttcaag 2220 ccggagttca tcaaccggct cgacgacgtg ctcatctttg agggtctcaa ccccgaagag 2280 ctggtgcgca tcgtcgacat ccagctggcg cagctgggca agcggctggc gcagcggcgg 2340 ctgcagctgc aggtctcgct gccggccaag cgctggttgg cgcagcgcgg attcgacccg 2400 gtgtacgggg cgcggccgtt gcgccggctg gtgcagcagg ccatcggtga ccagctggcc 2460 aagatgctgt tggccggcca ggtgcacgac ggcgataccg tgccggtcaa cgtcagcccc 2520 gacgccgact cgctgatcct gggc 2544 77 182 DNA Mycobacterium tuberculosis 77 gtcctggcac gccacgacgg cggccgcctg ggtgggttca accgggtcag gtcgatacgt 60 cgcgaagctc acctcggcga acgtcggagg cggccgcagt tgggcgatca gccgcaccgg 120 agacacggtc ggatgcctgt ccaccaggtg gtccaccgaa ccgcaagctt cggaggcaga 180 cc 182 78 258 PRT Mycobacterium tuberculosis 78 Met Pro Asp Ser Gly Gln Leu Gly Ala Ala Asp Thr Pro Leu Arg Leu 1 5 10 15 Leu Ser Ser Val His Tyr Leu Thr Asp Gly Glu Leu Pro Gln Leu Tyr 20 25 30 Asp Tyr Pro Asp Asp Gly Thr Trp Leu Arg Ala Asn Phe Ile Ser Ser 35 40 45 Leu Asp Gly Gly Ala Thr Val Asp Gly Thr Ser Gly Ala Met Ala Gly 50 55 60 Pro Gly Asp Arg Phe Val Phe Asn Leu Leu Arg Glu Leu Ala Asp Val 65 70 75 80 Ile Val Val Gly Val Gly Thr Val Arg Ile Glu Gly Tyr Ser Gly Val 85 90 95 Arg Met Gly Val Val Gln Arg Gln His Arg Gln Ala Arg Gly Gln Ser 100 105 110 Glu Val Pro Gln Leu Ala Ile Val Thr Arg Ser Gly Arg Leu Asp Arg 115 120 125 Asp Met Ala Val Phe Thr Arg Thr Glu Met Ala Pro Leu Val Leu Thr 130 135 140 Thr Thr Ala Val Ala Asp Asp Thr Arg Gln Arg Leu Ala Gly Leu Ala 145 150 155 160 Glu Val Ile Ala Cys Ser Gly Asp Asp Pro Gly Thr Val Asp Glu Ala 165 170 175 Val Leu Val Ser Gln Leu Ala Ala Arg Gly Leu Arg Arg Ile Leu Thr 180 185 190 Glu Gly Gly Pro Thr Leu Leu Gly Thr Phe Val Glu Arg Asp Val Leu 195 200 205 Asp Glu Leu Cys Leu Thr Ile Ala Pro Tyr Val Val Gly Gly Leu Ala 210 215 220 Arg Arg Ile Val Thr Gly Pro Gly Gln Val Leu Thr Arg Met Arg Cys 225 230 235 240 Ala His Val Leu Thr Asp Asp Ser Gly Tyr Leu Tyr Thr Arg Tyr Val 245 250 255 Lys Thr 79 774 DNA Mycobacterium tuberculosis 79 atgcccgact ctggtcagct cggagccgct gacaccccgc taaggctgct cagctcggtg 60 cattacctca ccgacggcga actcccccag ctttacgact atccggatga cggcacctgg 120 ttgcgggcga acttcatcag cagcttggac ggcggcgcta ccgtcgatgg caccagcggg 180 gcgatggccg ggcccggcga ccgattcgtc ttcaacctgt tgcgtgaact tgccgacgtc 240 atcgtggtcg gcgtgggcac cgtgcgcatt gagggctact ccggcgtccg gatgggtgtc 300 gtccagcgcc agcaccggca ggcccgaggc caaagcgaag ttccgcaact ggcaatcgtc 360 accaggtccg gtcgccttga ccgtgacatg gcggtattca cccggaccga gatggcaccg 420 ttggtgctca ccaccacggc ggtcgccgat gacacgcgcc agcggctcgc gggcctcgcc 480 gaggtgatcg cgtgctccgg cgacgatccg ggcacggtcg atgaggcagt gctcgtgtcc 540 cagctcgcgg ctcgcggtct gcgccggatc cttaccgaag gcgggccgac gttgctcggg 600 acattcgtcg agcgtgacgt gctcgacgag ctgtgtctga cgatcgcccc ctacgtcgtc 660 ggcggcctgg cgcgccgcat agtgacggga cccgggcagg tgctgacccg gatgcgctgt 720 gcccatgtcc tcaccgacga ctccggctac ctgtacaccc gctacgtcaa gacc 774 80 528 PRT Mycobacterium tuberculosis 80 Met Ala Thr Val Val Gly Met Ser Arg Pro Met Thr Ser Thr Ala Met 1 5 10 15 Leu Val Ala Leu Thr Cys Ser Ala Thr Val Leu Ala Ala Cys Val Pro 20 25 30 Ala Phe Gly Ala Asp Pro Arg Phe Ala Thr Tyr Ser Gly Ala Gly Pro 35 40 45 Gln Gly Ala Ala Thr Thr Thr Pro Pro Pro Ala Gly Pro Pro Pro Leu 50 55 60 Ala Ala Pro Lys Asn Asp Leu Ser Trp His Asp Cys Thr Ser Arg Val 65 70 75 80 Tyr Ser Asn Ala Gly Ile Pro Ala Ala Pro Gly Val Lys Leu Glu Cys 85 90 95 Ala Ser Tyr Asp Thr Asp Leu Asp Pro Leu Val Gly Gly Ser Thr Ala 100 105 110 Val Ser Ile Gly Val Val Arg Ala Arg Ser Asn Gln Thr Pro Ser Asp 115 120 125 Ala Gly Pro Leu Val Phe Thr Thr Gly Ser Asp Leu Pro Ser Ser Thr 130 135 140 Gln Leu Pro Val Trp Leu Ala His Ala Gly Ile Asp Val Leu Arg Ser 145 150 155 160 His Pro Ile Val Ala Val Asp Arg Arg Gly Met Gly Met Ser Ser Pro 165 170 175 Ile Asp Cys Arg Asp His Phe Asp Arg Asp Glu Met Arg Asp Gln Ala 180 185 190 Gln Phe Gln Ala Gly Asp Asp Pro Val Ala Asn Leu Ser Asp Ile Ser 195 200 205 Asn Thr Ala Thr Thr Asp Cys Thr Asp Ala Ile Ala Pro Gly Glu Ser 210 215 220 Ala Tyr Asp Asn Thr His Ala Ala Ser Asp Ile Glu Arg Leu Arg Lys 225 230 235 240 Leu Trp Asp Val Pro Ala Leu Ala Phe Val Gly Ile Gly Asn Gly Thr 245 250 255 Gln Val Ala Leu Ala Tyr Ala Ala Ser Arg Pro Asp Asn Val Ala Arg 260 265 270 Leu Ile Leu Asp Ser Pro Ile Ala Leu Gly Val Ser Ala Glu Ala Ala 275 280 285 Ala Glu Gln Gln Val Gln Gly Gln Gln Ala Ala Leu Asp Ala Phe Ala 290 295 300 Ala Gln Cys Val Ala Val Asn Cys Ala Leu Gly Ser His Pro Lys Gly 305 310 315 320 Ala Val Ser Ala Leu Leu Ser Ala Ala Arg Ser Gly Asp Gly Pro Gly 325 330 335 Gly Ala Ser Val Ala Ala Val Ala Asn Ala Val Ala Thr Ala Leu Gly 340 345 350 Phe Pro Asp Ser Gly Arg Val Asp Ser Thr Thr Lys Leu Ala Asp Ala 355 360 365 Leu Ala Ala Ala Arg Ser Gly Asp Met Asn Leu Leu Ser Ala Leu Ile 370 375 380 Asn Arg Ala Asp Thr Thr Arg Asp Thr Asp Gly Gln Phe Ile Ser Ser 385 390 395 400 Cys Ser Asp Ala Val Asn Arg Pro Thr Pro Asp Arg Val Arg Glu Leu 405 410 415 Val Val Ala Trp Gly Lys Leu Tyr Pro Gln Phe Gly Ala Val Ala Ala 420 425 430 Leu Asn Leu Val Lys Cys Val His Trp Pro Ser Ser Ser Pro Pro Gln 435 440 445 Pro Pro Lys Asp Leu Lys Val Asp Val Leu Leu Leu Gly Val Gln Asn 450 455 460 Asp Pro Ile Val Gly Asn Glu Gly Val Ala Ala Thr Ala Ala Thr Ala 465 470 475 480 Ile Asn Ala Asn Ala Ala Ser Lys Arg Val Met Trp Gln Gly Ile Gly 485 490 495 His Gly Ala Ser Ile Tyr Ser Ser Cys Ala Val Pro Pro Leu Val Ala 500 505 510 Tyr Leu Asp Thr Gly Lys Leu Pro Asp Thr Asp Thr Tyr Cys Pro Ala 515 520 525 81 1584 DNA Mycobacterium tuberculosis 81 atggctactg tggtcggcat gagtcggccc atgacgtcaa ccgcgatgtt ggtcgcgctg 60 acctgctcgg cgacagtgct ggccgcatgc gtcccggcgt tcggcgccga cccgcggttc 120 gcgacctact cgggcgcagg accgcaaggc gcagccacca cgacaccacc gccggctggc 180 ccaccaccgc tcgccgcacc caagaacgac ttgtcgtggc acgactgcac gtcacgggtg 240 tactcgaatg ctgggatccc agcagcgccc ggcgtcaagc tggaatgcgc aagctatgac 300 accgacctcg acccgctcgt cggcgggtcc acagcggtaa gcatcggcgt agtgcgcgcg 360 cgctccaacc agaccccgag cgacgcagga cccctggtgt tcaccaccgg ctccgaccta 420 ccctcgtcga cgcagttgcc ggtctggctg gcacacgcgg gcatcgatgt gctccgcagc 480 caccccattg tcgccgtcga ccgccgcggc atgggcatgt cgagcccaat cgactgccgc 540 gatcactttg accgcgacga gatgcgtgat caggcgcaat tccaggctgg cgacgatccg 600 gtggccaacc tttccgacat ctccaacacc gccaccaccg actgcaccga cgccatcgcg 660 ccaggcgagt ccgcctacga caacacccac gccgcctcgg atatcgagcg cttacgcaaa 720 ctctgggacg tccctgccct cgccttcgtc ggcattggca acggcaccca agtggcgctg 780 gcctacgcag catcgcgtcc cgacaacgtc gccagactga tcctcgactc cccaatcgcg 840 ttgggggtct ctgccgaagc cgccgccgag caacaggtcc agggccaaca ggcggcgctg 900 gacgcattcg ctgcgcaatg tgtcgcggtg aactgcgcgc tgggctccca tccgaaaggc 960 gcggtcagcg cgctgctgtc ggccgcccgg tccggtgatg ggcccggcgg cgcgtcggtg 1020 gcggctgtcg ccaacgccgt cgccaccgcg ttgggcttcc ccgacagtgg ccgggtcgat 1080 agcaccacga aattggccga cgcgctggcc gcggcccgct ccggggacat gaacttgctg 1140 tccgccctga tcaaccgcgc cgataccacc cgggatacgg acggtcagtt catcagctcg 1200 tgcagcgatg cggtcaaccg cccgacaccg gaccgggtgc gcgagctggt ggtggcttgg 1260 gggaagctct acccgcagtt cggcgccgtc gcggcgctca acctggtgaa atgcgtgcac 1320 tggcccagca gttcgccgcc gcagccaccg aaagacctca aggtcgacgt gctgttgctc 1380 ggtgtgcaaa acgacccgat cgtgggcaac gaaggggtcg ccgcgaccgc cgccacggcc 1440 atcaacgcca acgccgccag caagcgggtg atgtggcaag gtattggcca cggcgccagc 1500 atctactcgt cctgcgcggt gccgccactc gtcgcctacc tggacactgg caagctgcct 1560 gacaccgaca cctattgccc cgcc 1584 82 433 PRT Mycobacterium tuberculosis 82 Val Tyr Gly Ala Leu Val Thr Ala Ala Asp Ser Ile Arg Thr Gly Leu 1 5 10 15 Gly Ala Ser Leu Leu Ala Gly Phe Arg Pro Arg Thr Gly Ala Pro Ser 20 25 30 Thr Ala Thr Ile Leu Arg Ser Ala Leu Trp Pro Ala Ala Val Leu Ser 35 40 45 Val Leu His Arg Ser Ile Val Leu Thr Thr Asn Gly Asn Ile Thr Asp 50 55 60 Asp Phe Lys Pro Val Tyr Arg Ala Val Leu Asn Phe Arg Arg Gly Trp 65 70 75 80 Asp Ile Tyr Asn Glu His Phe Asp Tyr Val Asp Pro His Tyr Leu Tyr 85 90 95 Pro Pro Gly Gly Thr Leu Leu Met Ala Pro Phe Gly Tyr Leu Pro Phe 100 105 110 Ala Pro Ser Arg Tyr Leu Phe Ile Ser Ile Asn Thr Ala Ala Ile Leu 115 120 125 Val Ala Ala Tyr Leu Leu Leu Arg Met Phe Asn Phe Thr Leu Thr Ser 130 135 140 Val Ala Ala Pro Ala Leu Ile Leu Ala Met Phe Ala Thr Glu Thr Val 145 150 155 160 Thr Asn Thr Leu Val Phe Thr Asn Ile Asn Gly Cys Ile Leu Leu Leu 165 170 175 Glu Val Leu Phe Leu Arg Trp Leu Leu Asp Gly Arg Ala Ser Arg Gln 180 185 190 Trp Cys Gly Gly Leu Ala Ile Gly Leu Thr Leu Val Leu Lys Pro Leu 195 200 205 Leu Gly Pro Leu Leu Leu Leu Pro Leu Leu Asn Arg Gln Trp Arg Ala 210 215 220 Leu Val Ala Ala Val Val Val Pro Val Val Val Asn Val Ala Ala Leu 225 230 235 240 Pro Leu Val Ser Asp Pro Met Ser Phe Phe Thr Arg Thr Leu Pro Tyr 245 250 255 Ile Leu Gly Thr Arg Asp Tyr Phe Asn Ser Ser Ile Leu Gly Asn Gly 260 265 270 Val Tyr Phe Gly Leu Pro Thr Trp Leu Ile Leu Phe Leu Arg Ile Leu 275 280 285 Phe Thr Ala Ile Thr Phe Gly Ala Leu Trp Leu Leu Tyr Arg Tyr Tyr 290 295 300 Arg Thr Gly Asp Pro Leu Phe Trp Phe Thr Thr Ser Ser Gly Val Leu 305 310 315 320 Leu Leu Trp Ser Trp Leu Val Met Ser Leu Ala Gln Gly Tyr Tyr Ser 325 330 335 Met Met Leu Phe Pro Phe Leu Met Thr Val Val Leu Pro Asn Ser Val 340 345 350 Ile Arg Asn Trp Pro Ala Trp Leu Gly Val Tyr Gly Phe Met Thr Leu 355 360 365 Asp Arg Trp Leu Leu Phe Asn Trp Met Arg Trp Gly Arg Ala Leu Glu 370 375 380 Tyr Leu Lys Ile Thr Tyr Gly Trp Ser Leu Leu Leu Ile Val Thr Phe 385 390 395 400 Thr Val Leu Tyr Phe Arg Tyr Leu Asp Ala Lys Ala Asp Asn Arg Leu 405 410 415 Asp Gly Gly Ile Asp Pro Ala Trp Leu Thr Pro Glu Arg Glu Gly Gln 420 425 430 Arg 83 1299 DNA Mycobacterium tuberculosis 83 gtgtacggtg cgctggtgac ggcagctgac tccatccgaa ccggcctagg cgcatccttg 60 ttggccggat tccgtccgcg caccggcgcc ccgagcaccg cgacgatcct gcggtcggcg 120 ctctggccgg ccgccgtcct gtcggtgctg caccgcagca tcgtattgac gaccaacggc 180 aacatcaccg acgatttcaa gccggtctac cgcgcggtgc tgaacttccg gcgcggatgg 240 gacatctata acgagcactt cgactacgtc gacccgcact acctgtatcc ccccggtggc 300 accctgctga tggcgccgtt cggctacctg cccttcgccc cgtcgcgcta tctgtttatc 360 tcgatcaaca ccgcggccat cctggtcgcc gcctacctgc tgctgcggat gttcaacttc 420 acgctgacct cggtggccgc acccgccctg attctggcca tgtttgctac cgagaccgtg 480 accaacacgc tggtgttcac caacatcaac ggctgcatcc tgctgttgga ggtgctcttt 540 ctgagatggc tgttggacgg ccgagccagt cgtcagtggt gcggcggcct ggcgatcggg 600 ctgaccctgg ttctcaaacc cctgctcggt ccgctgttgt tgctgccgct gctgaaccgc 660 cagtggcggg ctctggtggc cgccgtcgtc gttcccgtcg tcgtcaacgt ggccgcgctg 720 ccgctggtca gtgacccgat gagcttcttc acccgcacgc tgccctacat cttgggcacc 780 cgggactact tcaacagctc gatcttgggc aacggcgtct acttcgggct gcccacctgg 840 ctgatcctgt tcctgcggat cctgttcacc gcgatcacct tcggcgcatt gtggctgttg 900 taccgctact accgcaccgg tgacccgctg ttttggttca ccacctcgtc gggtgtgctg 960 ctgctgtggt cgtggctggt gatgtcgctg gcccagggct actactcgat gatgctgttc 1020 ccgttcctga tgaccgttgt gctgcccaac tcggtgatcc gcaactggcc ggcgtggctg 1080 ggagtctacg gcttcatgac gttggatcgc tggctgctgt tcaactggat gagatggggc 1140 cgcgcgctgg aatacctcaa gatcacctac ggttggtcgt tgctgttgat cgtgacgttt 1200 accgtgctct atttccgcta tctggacgcc aaggcggaca accggctgga cggcggtatc 1260 gatccagcct ggctgacgcc cgagcgggag ggccagcgg 1299 84 314 DNA Mycobacterium tuberculosis 84 tctccttgtc aggcttgacg ggtcgcaccc gcgaacaccc ctctgtgata gcacgagtta 60 tcaggaggtt cggcggggcg ttacctttgc ggttgtgcac ttcgactggg agcgcctgac 120 cgacagcgtg catcgctgcc ggctgccgtt ctgtgacgtc accgttgggc tggtccgggg 180 ccgcaccgga atactgctcg tcgacaccgg gaccaccctc ggcgaagcaa cagcaatcgc 240 ggccgacgtc aagcagatcg ctggttgcca ggtaacgcat gttgtgttga cacacaagca 300 tttcgaccat gtgc 314 85 197 PRT Mycobacterium tuberculosis 85 Val Ala His Ala Phe His Arg Phe Ala Leu Ala Ile Leu Gly Leu Ala 1 5 10 15 Leu Pro Val Ala Leu Val Ala Tyr Gly Gly Asn Gly Asp Ser Arg Lys 20 25 30 Ala Ala Pro Leu Ala Pro Lys Ala Ala Ala Leu Gly Arg Ser Met Pro 35 40 45 Glu Thr Pro Thr Gly Asp Val Leu Thr Ile Ser Ser Pro Ala Phe Ala 50 55 60 Asp Gly Ala Pro Ile Pro Glu Gln Tyr Thr Cys Lys Gly Ala Asn Ile 65 70 75 80 Ala Pro Pro Leu Thr Trp Ser Ala Pro Phe Gly Gly Ala Leu Val Val 85 90 95 Asp Asp Pro Asp Ala Pro Arg Glu Pro Tyr Val His Trp Ile Val Ile 100 105 110 Gly Ile Ala Pro Gly Ala Gly Ser Thr Ala Asp Gly Glu Thr Pro Gly 115 120 125 Gly Gly Ile Ser Leu Pro Asn Ser Ser Gly Gln Pro Ala Tyr Thr Gly 130 135 140 Pro Cys Pro Pro Ala Gly Thr Gly Thr His His Tyr Arg Phe Thr Leu 145 150 155 160 Tyr His Leu Pro Ala Val Pro Pro Leu Ala Gly Leu Ala Gly Thr Gln 165 170 175 Ala Ala Arg Val Ile Ala Gln Ala Ala Thr Met Gln Ala Arg Leu Ile 180 185 190 Gly Thr Tyr Glu Gly 195 86 591 DNA Mycobacterium tuberculosis 86 gtggcgcacg catttcaccg gttcgcactg gccatcttgg ggctggcgct ccccgtggcg 60 ctagttgcct acggtggcaa cggtgacagt cgaaaggcgg cgccgctggc gccgaaagca 120 gcagcgctcg gtcggagtat gcccgaaacg cctaccggcg atgtactgac aatcagcagt 180 ccggcattcg ccgacggtgc gccgatcccg gaacagtaca cctgcaaagg agccaatatc 240 gcgcctccgt tgacctggtc ggcgccgttt ggcggcgcac tcgttgtcga tgatccggac 300 gcacctcgcg aaccttacgt ccattggatc gtgatcggga tcgcccctgg tgctggcagc 360 accgccgatg gtgagactcc cggtggcgga atcagcctgc cgaactccag cggtcagccc 420 gcatacaccg gcccctgccc gccggcgggc accgggacac accactaccg gtttaccctc 480 taccaccttc ctgccgtgcc tccactcgcg ggactggctg ggacacaagc ggcgcgggtg 540 atcgcgcagg ccgccaccat gcaggcccgg ctcatcggaa catacgaagg c 591 87 201 PRT Mycobacterium tuberculosis 87 Met Thr Ser Thr Leu His Arg Thr Pro Leu Ala Thr Ala Gly Leu Ala 1 5 10 15 Leu Val Val Ala Leu Gly Gly Cys Gly Gly Gly Gly Gly Asp Ser Arg 20 25 30 Glu Thr Pro Pro Tyr Val Pro Lys Ala Thr Thr Val Asp Ala Thr Thr 35 40 45 Pro Ala Pro Ala Ala Glu Pro Leu Thr Ile Ala Ser Pro Met Phe Ala 50 55 60 Asp Gly Ala Pro Ile Pro Val Gln Phe Ser Cys Lys Gly Ala Asn Val 65 70 75 80 Ala Pro Pro Leu Thr Trp Ser Ser Pro Ala Gly Ala Ala Glu Leu Ala 85 90 95 Leu Val Val Asp Asp Pro Asp Ala Val Gly Gly Leu Tyr Val His Trp 100 105 110 Ile Val Thr Gly Ile Ala Pro Gly Ser Gly Ser Thr Ala Asp Gly Gln 115 120 125 Thr Pro Ala Gly Gly His Ser Val Pro Asn Ser Gly Gly Arg Gln Gly 130 135 140 Tyr Phe Gly Pro Cys Pro Pro Ala Gly Thr Gly Thr His His Tyr Arg 145 150 155 160 Phe Thr Leu Tyr His Leu Pro Val Ala Leu Gln Leu Pro Pro Gly Ala 165 170 175 Thr Gly Val Gln Ala Ala Gln Ala Ile Ala Gln Ala Ala Ser Gly Gln 180 185 190 Ala Arg Leu Val Gly Thr Phe Glu Gly 195 200 88 603 DNA Mycobacterium tuberculosis 88 atgacgagca cacttcaccg aaccccatta gccaccgcgg ggctggcgct cgtagtggcg 60 ctgggtggct gcgggggcgg gggcggtgac agtcgagaga caccgccata cgtgccgaaa 120 gcgacgaccg tcgacgcaac aacgccggcg ccggccgccg agccactgac gatcgccagt 180 cccatgttcg ccgacggcgc cccgatcccg gtgcaattca gctgcaaggg ggccaacgtg 240 gcgccaccgt tgacgtggtc gtcgcccgcg ggcgcagccg aactggcact cgtcgtcgat 300 gaccccgacg cggtcggcgg actgtacgtg cactggatcg tgaccggaat cgcccctggc 360 tctggcagca cggcggatgg tcagactcct gctggtgggc acagcgtgcc gaattctggt 420 ggtcggcaag gatacttcgg tccatgcccg ccggcgggca ccgggacaca ccactaccgg 480 tttaccctct accaccttcc tgtcgcgctc cagctgccac cgggagccac gggagtccaa 540 gcggcacagg cgatagcaca ggccgccagc ggacaggccc ggctcgtcgg cacattcgaa 600 ggc 603 89 334 PRT Mycobacterium tuberculosis 89 Met Arg Ala Val Val Ile Thr Lys His Gly Asp Pro Ser Val Leu Gln 1 5 10 15 Val Arg Gln Arg Pro Asp Pro Pro Pro Pro Gly Pro Gly Gln Leu Arg 20 25 30 Val Ala Val Arg Ala Ala Gly Val Asn Phe Ala Asp His Leu Ala Arg 35 40 45 Val Gly Leu Tyr Pro Asp Ala Pro Lys Leu Pro Ala Val Val Gly Tyr 50 55 60 Glu Val Ala Gly Thr Val Glu Ala Val Gly Asp Gly Val Asp Pro Asn 65 70 75 80 Arg Val Gly Glu Arg Val Leu Ala Gly Thr Arg Phe Gly Gly Tyr Cys 85 90 95 Glu Ile Val Asn Val Ala Ala Thr Asp Ser Val Val Leu Pro Asp Ala 100 105 110 Leu Ser Phe Glu Gln Gly Ala Ala Val Pro Val Asn Tyr Ala Thr Ala 115 120 125 Trp Ala Ala Leu His Gly Tyr Gly Ser Leu Arg Ala Gly Glu Arg Val 130 135 140 Leu Ile His Ala Ala Ala Gly Gly Val Gly Ile Ala Ala Val Gln Phe 145 150 155 160 Ala Lys Ala Ala Lys Ala Glu Val His Gly Thr Ala Ser Pro Gln Lys 165 170 175 His Gln Lys Leu Ala Glu Phe Gly Val Asp Arg Ala Ile Asp Tyr Arg 180 185 190 Arg Asp Gly Trp Trp Gln Gly Leu Gly Pro Tyr Asp Val Val Leu Asp 195 200 205 Ala Leu Gly Gly Thr Ser Leu Arg Arg Ser Tyr Thr Leu Leu Arg Pro 210 215 220 Gly Gly Arg Leu Val Gly Tyr Gly Ile Ser Asn Met Gln His Gly Glu 225 230 235 240 Lys Arg Ser Met Arg Arg Val Ala Pro His Ala Leu Ser Met Leu Arg 245 250 255 Gly Phe Asn Leu Met Lys Gln Leu Glu Glu Ser Lys Thr Val Ile Gly 260 265 270 Leu Asn Met Leu Arg Leu Trp Asp Asp Arg Arg Thr Leu Glu Pro Trp 275 280 285 Ile Ala Pro Leu Thr Lys Ala Leu Asn Asp Gly Thr Ile Leu Pro Ile 290 295 300 Val His Ala Ile Val Pro Phe Ala Glu Ala Pro Glu Ala His Arg Ile 305 310 315 320 Leu Ala Ala Arg Glu Asn Val Asp Lys Val Val Leu Val Pro 325 330 90 1002 DNA Mycobacterium tuberculosis 90 atgcgagcag tggtcatcac caaacatggc gacccatcgg tcttgcaggt gcggcagcga 60 ccggacccgc cgccaccggg cccgggccag ctgcgggtcg ccgtccgcgc agcaggggtg 120 aacttcgctg accatctcgc ccgcgtcggc ctgtacccag acgcgccgaa acttccggcg 180 gtggtcggat acgaagtcgc tgggacggtc gaggctgtcg gtgatggggt cgacccgaac 240 cgggtcggcg aacgagtcct ggccggtaca cgatttggtg gctactgcga gatcgtcaac 300 gttgcggcca ccgactcggt tgtgctcccc gatgcgctga gcttcgaaca gggtgccgcg 360 gtcccggtga attacgcgac cgcctgggcg gcgctgcacg gctacggatc gttgcgcgcc 420 ggtgagcggg tgctgattca cgccgcggcc ggtggagtcg gcatcgcggc ggtccaattc 480 gcgaaagcag ccaaggccga agtgcacggc accgcatcac cccaaaaaca tcagaagctg 540 gccgagttcg gtgtggaccg cgcgatcgac taccgccggg acggctggtg gcagggattg 600 ggcccgtatg acgtcgtgct tgacgcgctc ggcggcacct cgctgcggcg gtcctacact 660 ctgctgcgcc cgggtggaag gctggttggc tacgggattt cgaatatgca gcacggcgag 720 aaacgatcga tgcgcagggt ggcgccccac gcgttgtcaa tgctgcgcgg ctttaacctg 780 atgaaacaac tcgaggagtc gaaaaccgtg atcggtctta acatgctgcg gttgtgggac 840 gatcgccgca cccttgaacc ctggatcgcg ccgctgacca aggcgctcaa cgacggaacg 900 atcctgccga tcgttcatgc aatcgtgccg ttcgccgaag ctcctgaagc acatcggatt 960 ctggccgcac gggagaacgt cgacaaggtg gtgctggtac cg 1002 91 145 DNA Mycobacterium tuberculosis 91 gtcagtcact tggctcacag tggggcacct gctttcctcg agttcttcta tgctccgaca 60 ctaaccaacc aggctggctg tttcgcggtc acgcaccccc tgaaaccggc gcgttcgctt 120 acagcgtcat acggtcacgt tgtcg 145 92 200 PRT Mycobacterium tuberculosis 92 Val Ser Gln Val Thr Asp Met Arg Ser Asn Ser Gln Gly Leu Ser Leu 1 5 10 15 Thr Asp Ser Val Tyr Glu Arg Leu Leu Ser Glu Arg Ile Ile Phe Leu 20 25 30 Gly Ser Glu Val Asn Asp Glu Ile Ala Asn Arg Leu Cys Ala Gln Ile 35 40 45 Leu Leu Leu Ala Ala Glu Asp Ala Ser Lys Asp Ile Ser Leu Tyr Ile 50 55 60 Asn Ser Pro Gly Gly Ser Ile Ser Ala Gly Met Ala Ile Tyr Asp Thr 65 70 75 80 Met Val Leu Ala Pro Cys Asp Ile Ala Thr Tyr Ala Met Gly Met Ala 85 90 95 Ala Ser Met Gly Glu Phe Leu Leu Ala Ala Gly Thr Lys Gly Lys Arg 100 105 110 Tyr Ala Leu Pro His Ala Arg Ile Leu Met His Gln Pro Leu Gly Gly 115 120 125 Val Thr Gly Ser Ala Ala Asp Ile Ala Ile Gln Ala Glu Gln Phe Ala 130 135 140 Val Ile Lys Lys Glu Met Phe Arg Leu Asn Ala Glu Phe Thr Gly Gln 145 150 155 160 Pro Ile Glu Arg Ile Glu Ala Asp Ser Asp Arg Asp Arg Trp Phe Thr 165 170 175 Ala Ala Glu Ala Leu Glu Tyr Gly Phe Val Asp His Ile Ile Thr Arg 180 185 190 Ala His Val Asn Gly Glu Ala Gln 195 200 93 600 DNA Mycobacterium tuberculosis 93 gtgagccaag tgactgacat gcgttcgaac tcgcagggtc ttagcctcac ggattcggtc 60 tacgagcgct tgctctccga gcgcatcatc ttcctgggct cggaggtgaa cgacgagatc 120 gccaaccggt tatgcgctca gattctgctg ctggccgccg aagacgccag caaggacatc 180 agcctctaca tcaattcgcc gggtggatcg atcagcgccg gcatggcgat ctacgacacc 240 atggtgctgg cgccctgtga catcgccacc tacgcgatgg gcatggccgc ctcgatgggc 300 gagttcctgc tggcggcagg taccaagggc aagcgctacg cgctgccgca tgctcgcatc 360 ctgatgcacc agccgttggg cggggtgacc ggcagcgcgg ccgatatcgc catccaggcc 420 gagcagttcg ccgtgatcaa gaaagaaatg ttccggctca acgccgaatt caccggccag 480 ccgatcgagc gcattgaggc ggattccgat cgcgaccgct ggttcaccgc cgccgaagcc 540 ctggaatacg gtttcgtcga tcacatcatc acccgcgccc acgtcaatgg agaagcacag 600 94 214 PRT Mycobacterium tuberculosis 94 Val Asn Ser Gln Asn Ser Gln Ile Gln Pro Gln Ala Arg Tyr Ile Leu 1 5 10 15 Pro Ser Phe Ile Glu His Ser Ser Phe Gly Val Lys Glu Ser Asn Pro 20 25 30 Tyr Asn Lys Leu Phe Glu Glu Arg Ile Ile Phe Leu Gly Val Gln Val 35 40 45 Asp Asp Ala Ser Ala Asn Asp Ile Met Ala Gln Leu Leu Val Leu Glu 50 55 60 Ser Leu Asp Pro Asp Arg Asp Ile Thr Met Tyr Ile Asn Ser Pro Gly 65 70 75 80 Gly Gly Phe Thr Ser Leu Met Ala Ile Tyr Asp Thr Met Gln Tyr Val 85 90 95 Arg Ala Asp Ile Gln Thr Val Cys Leu Gly Gln Ala Ala Ser Ala Ala 100 105 110 Ala Val Leu Leu Ala Ala Gly Thr Pro Gly Lys Arg Met Ala Leu Pro 115 120 125 Asn Ala Arg Val Leu Ile His Gln Pro Ser Leu Ser Gly Val Ile Gln 130 135 140 Gly Gln Phe Ser Asp Leu Glu Ile Gln Ala Ala Glu Ile Glu Arg Met 145 150 155 160 Arg Thr Leu Met Glu Thr Thr Leu Ala Arg His Thr Gly Lys Asp Ala 165 170 175 Gly Val Ile Arg Lys Asp Thr Asp Arg Asp Lys Ile Leu Thr Ala Glu 180 185 190 Glu Ala Lys Asp Tyr Gly Ile Ile Asp Thr Val Leu Glu Tyr Arg Lys 195 200 205 Leu Ser Ala Gln Thr Ala 210 95 642 DNA Mycobacterium tuberculosis 95 gtgaattccc aaaattctca gatccagccc caggcgcgct acatcctgcc gtcgttcatc 60 gagcactcca gcttcggggt caaggagtcc aatccataca acaagctgtt cgaggaacgc 120 atcatcttcc tcggcgtcca ggtcgacgac gcgtcggcga acgacatcat ggcacagttg 180 ctggtgttgg agtcgttgga tcccgaccgc gatatcacca tgtacatcaa ctcgccgggc 240 ggtgggttca cctcgctgat ggcgatctac gacaccatgc aatacgtgcg ggccgatatc 300 cagacggtgt gtctgggcca ggccgcctcg gcggctgcgg tgctgctggc cgccggaaca 360 ccgggcaagc gcatggcgct gccgaatgcg cgggtgttga tccatcagcc gtcgttgtcg 420 ggcgtgatcc agggacagtt ctccgatctg gagatccagg ccgccgagat cgagcggatg 480 cgcaccctga tggaaaccac gctggcccgc cacaccggca aggacgccgg agtgatccgc 540 aaagacactg accgggacaa gatcttgacc gcggaagagg ctaaggacta cggcatcatc 600 gacacggtgc tcgagtaccg gaagctctcc gcgcaaaccg cc 642 96 381 DNA Mycobacterium tuberculosis 96 ccatttacca acacattcgg gctcaggatt gtttagcgta ctaacttcat ggtagtggct 60 caagacgaaa gcatcgcatg ctgcaaggtc cgatacaacg ggaaaactgt tgtgggactt 120 gttaatctgc aggccacagc acgacgaaga acacattatc cagccaactc acaggccgtt 180 gccatgccgc taccagacgt cgtaggcctg ggaaagttaa ggtagcaaca ctgctcgaca 240 gccacagcag catgcaccgc gcgtgtgatc cgcacgagcc gcacgggcgc gagcagacgc 300 aaaaggcccc gaaatccgtt ggattcgggg ccttttgcgt ctttcgcgcc caacgtgggt 360 gcttggctag ggtgaatcct t 381 97 939 PRT Mycobacterium tuberculosis 97 Val Asp Pro His Arg Asp Leu Glu Ser Arg Ala Phe Ala Gly Asn Trp 1 5 10 15 Arg Val Tyr Gln Gln Gln Ala Leu Asp Ala Phe Asp Ala Asp Val Ala 20 25 30 Ala Gly Asp Asn Arg Ala Tyr Leu Val Leu Pro Pro Gly Ala Gly Lys 35 40 45 Thr Met Ile Gly Leu Glu Ala Ala Arg Arg Leu Gly Arg Arg Ser Leu 50 55 60 Val Leu Val Pro Asn Thr Ala Val Gln Ala Gln Trp Ala Ala Ala Trp 65 70 75 80 Asp Asn Ser Phe Pro Ser Ser Asp Arg Ser Ala Ser Lys Cys Gly Thr 85 90 95 Glu Arg Gly Leu Ala Ser Ala Met Asn Val Leu Thr Tyr Gln Ser Leu 100 105 110 Ala Val Ile Asp Ala Glu Thr Asp Ser Thr Val Arg Arg Glu Val Leu 115 120 125 Arg Asn Arg Asp Gln Gln Ala Leu Leu Asp Leu Leu His Pro Asn Gly 130 135 140 Arg Ala Val Ile Glu Arg Ala Ala Thr Leu Gly Pro Trp Thr Leu Val 145 150 155 160 Leu Asp Glu Cys His His Leu Leu Ala Thr Trp Gly Ala Leu Val Ser 165 170 175 Ala Leu Ala Ser Val Leu Gly Ala Gln Thr Ala Leu Ile Gly Leu Thr 180 185 190 Ala Thr Pro Ala Thr Glu Leu Thr Ala Trp Gln His Thr Leu His Asp 195 200 205 Glu Leu Phe Gly Thr Ala Asp Phe Val Ile Pro Thr Pro Ala Leu Val 210 215 220 Arg Glu Gly Asp Leu Ala Pro Tyr Gln Glu Leu Val Tyr Leu Thr Gln 225 230 235 240 Pro Thr Pro Glu Glu Gln Ala Trp Ile Gly Thr His Arg Ala Arg Phe 245 250 255 Ala Asp Leu Met Leu Ala Leu Ile Asp Gln Lys Val Gly Ser Met Ser 260 265 270 Leu Ala Ala Trp Leu His Thr Arg Ile Val Asp Arg Ala Thr Arg Glu 275 280 285 Gly Asn Gln Ile Ala Trp Ser Thr Phe Glu Arg Ala Glu Pro Asp Leu 290 295 300 Ala Cys Ser Gly Leu Arg Phe Ala Tyr Asp Gly Leu Ile Pro Leu Pro 305 310 315 320 Asp Gly Val Arg Leu Arg Glu Gln His Arg Ile Ala Pro Asp Ala Gln 325 330 335 Asp Trp Val Asn Val Leu Thr Asp Phe Ser Val Gly His Leu Gln Gln 340 345 350 Ser Ala Asp Pro Arg Asp Ala His Ala Leu Thr Ala Ile Lys Arg Val 355 360 365 Leu Pro Gly Leu Gly Tyr Arg Leu Thr Ser Arg Gly Val Arg Val Ala 370 375 380 Thr Ser Pro Val Asp Arg Leu Cys Ala Leu Ser Glu Ser Lys Ile Ala 385 390 395 400 Ala Thr Ala His Ile Leu Asp Thr Glu Asp Ala Val Leu Gly Ala Arg 405 410 415 Leu Arg Ala Leu Val Leu Cys Asp Phe Glu Ser Met Thr Gly Ala Leu 420 425 430 Pro Thr Ser Leu Lys Gly Ala Pro Val Ser Glu Gln Ser Gly Ser Ala 435 440 445 Gln Leu Val Ala Ala Met Leu Ala Ala Ser Asp His Arg Arg Arg Thr 450 455 460 Pro Leu His Ala Leu Leu Val Thr Gly Gln Thr Phe Ala Cys Pro Ala 465 470 475 480 Ala Ile Glu Asp Asp Leu Ile Ala Phe Cys Ala Glu Arg Gly Ala Leu 485 490 495 Val Thr Ala Glu Pro Leu Asp Ala His Pro Ser Leu Arg Val Met Arg 500 505 510 Gly Thr Gly Gly Phe Thr Pro Arg Thr Trp Val Ala Leu Ala Thr Glu 515 520 525 Tyr Phe Leu Ala Gly Arg Ala Arg Val Leu Val Gly Thr Arg Ser Leu 530 535 540 Leu Gly Glu Gly Trp Asp Cys Ala Ala Val Asn Val Asn Ile Asp Leu 545 550 555 560 Thr Ser Ala Thr Thr Gln Ala Ala Ile Thr Gln Met Arg Gly Arg Ala 565 570 575 Ile Arg Asn Asp Pro Ser Asp Gly His Lys Val Ala Asp Asn Trp Ser 580 585 590 Val Cys Cys Ile Ala Thr Glu His Pro Arg Gly Asp Ala Asp Tyr Leu 595 600 605 Arg Leu Val Arg Lys His Asp Gly Tyr Tyr Ala Ala Thr Pro Gln Gly 610 615 620 Leu Ile Glu Ser Gly Val Thr His Cys Asp Pro Ser Leu Ser Pro Tyr 625 630 635 640 Gly Pro Pro Val Thr Asp Thr His Ala Ile Thr Ala Arg Ala Leu Gln 645 650 655 Arg Val Ala Glu Arg Ala Gln Ala Arg Ser Trp Trp Arg Ile Gly Glu 660 665 670 Pro Tyr Glu Gly Val Asp Val Ala Thr Ile Arg Val Arg Ser Arg Gln 675 680 685 Pro Leu Gly Val Ala Ala Pro Arg Ile Pro Ala Ser Ala Leu Thr Pro 690 695 700 Pro Val Pro Gly Gln Phe Ser Pro Val Arg Leu Ala Arg Gly Ala Val 705 710 715 720 Ala Ala Val Ser Val Val Gly Ala Ser Thr Ala Thr Ala Val Ala Ser 725 730 735 Ala Asn Leu Gly Met Leu Ala Gly Ala Gly Thr Ala Gly Ala Ile Val 740 745 750 Ala Ala Gly Val Gly Leu Val Ala Thr Ala Ala Ala Ala Glu Ser Arg 755 760 765 Arg Leu Asp His Ala Pro Asn Ala Leu Glu Gln Leu Ala Ala Val Val 770 775 780 Ala Asp Ala Leu Tyr Ala Ala Gly Gly Ala Gln Arg Gly Ser Ala Ala 785 790 795 800 Leu Arg Leu Ala Ser Asp Pro Glu Gly Trp Ile Arg Cys Gln Leu Asp 805 810 815 Gly Val Pro Thr Glu Gln Ser Leu Arg Phe Thr Ala Ala Leu Asp Glu 820 825 830 Leu Leu Ala Pro Leu Ala Glu Pro Arg Tyr Leu Ile Gly Arg Lys Ile 835 840 845 Leu Thr Pro Pro Ala Arg Pro Val Ala Arg Arg Leu Phe Ala Val Arg 850 855 860 Ala Val Val Gly Leu Ser Leu Pro Gly Thr Val Ala Trp His Ala Val 865 870 875 880 Pro Arg Trp Phe Ala Arg Asn Lys Asp Arg Arg Gln His Leu Ala Gln 885 890 895 Ala Trp Arg Lys His Ile Gly Pro Pro Arg Gln Leu Pro Ala Asp Ser 900 905 910 Pro Gln Gly Gln Ala Ile Leu Asp Leu Phe Arg Gly Asp Asn Pro Leu 915 920 925 Ser Val Thr Thr Gln Leu Arg Thr Thr Trp Arg 930 935 98 2817 DNA Mycobacterium tuberculosis 98 gtggatcctc accgcgacct ggaatcgcgg gcctttgccg gcaactggcg ggtataccaa 60 cagcaagcgt tggacgcgtt cgacgccgac gtcgctgccg gcgacaaccg tgcctatctg 120 gtgctgccgc cgggtgcggg caagacgatg atcggcctgg aagcagcgcg ccggctgggg 180 cgccggagtt tggtgttggt tcccaacacg gcggtgcagg cgcagtgggc cgccgcgtgg 240 gataacagtt ttccgtcgtc ggaccggtcg gcatcgaagt gtggaaccga gcgtggcctt 300 gcctcggcga tgaacgtcct gacgtatcag tcgcttgccg tcatcgacgc cgaaaccgat 360 tcgacagtcc ggcgggaagt cctgcgcaac cgcgaccagc aagcgttgct ggatctcctg 420 caccccaacg ggagggcggt gatcgagcgg gcggcgacgc taggcccgtg gacgctggtg 480 ctcgatgagt gccaccatct gctagctacg tggggcgccc tggtcagtgc gttggcgtcg 540 gtcctcggag cgcagaccgc gctgatcggt ctaacggcga ccccggccac agagctcacc 600 gcgtggcagc acaccctgca tgatgagctg ttcggcaccg ccgacttcgt gatcccgaca 660 cccgctctgg ttagggaagg cgacctggct ccctaccaag agttggtcta tctgacccaa 720 ccgacgcccg aagagcaggc ctggatcggc acccaccggg cgcgcttcgc cgacctcatg 780 ctggccctca tcgaccaaaa ggtgggcagc atgtcgttgg ccgcgtggct gcacacccgg 840 atcgtggatc gagcgacgcg cgagggcaat cagatcgcct ggtcgacgtt cgagcgtgcc 900 gaacccgacc tcgcgtgcag cggcctgcgc ttcgcctacg acggcctgat tccactaccc 960 gacggcgtgc gcctgcgcga gcagcaccga attgcgcccg atgcccagga ctgggttaac 1020 gtattgaccg acttcagcgt cgggcacctg caacaaagcg cggatccgcg cgacgcgcac 1080 gcgctgaccg cgatcaagcg ggtgctaccc ggcctgggct accggctgac cagtcgcggc 1140 gtacgcgtcg cgacctcgcc agtagacaga ctgtgcgcgc tgtccgaatc caagatcgcc 1200 gcgaccgcgc acatcctcga caccgaggac gccgtcttgg gggcgcggtt gcgggcgctg 1260 gtgctctgcg atttcgaatc gatgaccggc gcccttccca catcgctgaa gggcgcaccc 1320 gtcagcgagc agtcgggttc ggcccagctg gttgccgcca tgctcgccgc gtcggatcac 1380 cgccgccgca ccccactgca cgcccttctg gtaacaggtc aaaccttcgc ctgcccggcc 1440 gcgatcgaag atgacctgat cgccttctgc gccgagcgcg gcgcgctcgt caccgccgag 1500 ccgcttgacg cccaccctag tctgcgggtc atgcgcggca ccggcggctt cacgccacgt 1560 acgtgggtcg cgctggctac cgaatacttc ctggccggcc gcgcccgcgt cctggtcggc 1620 acccgttcgc tactaggtga agggtgggac tgcgcggcgg tcaacgtcaa tatcgacctg 1680 acgagcgcaa ccacccaggc agcgatcact cagatgcgcg gccgcgccat ccgcaacgac 1740 ccctcggacg gtcacaaggt ggcggacaac tggtcggtct gctgtatcgc cacagaacac 1800 ccgcgcggtg atgccgacta cctgcgcctg gtgcgcaaac atgacgggta ctacgcggca 1860 accccgcagg ggctcatcga atcgggtgtg acgcactgcg atccgtcgct gtcgccgtac 1920 ggtcctccgg tcaccgatac ccacgccatc acggcgcgag cgctgcagcg cgtcgccgaa 1980 cgcgcccagg cgagatcctg gtggcgaatc ggcgagccct acgaaggagt cgacgtcgca 2040 accatccgcg tgcgctcccg ccagccgctc ggggtcgccg caccccgcat ccccgcctcg 2100 gcattgaccc caccggtgcc gggacagttc agtccggtcc gcctggcaag gggtgccgtg 2160 gccgccgttt ccgtggtcgg cgccagcacc gccaccgcag ttgcctccgc caatctcggc 2220 atgctggcgg gtgccggcac ggccggcgcc atcgtcgcgg cgggtgttgg cctggtggca 2280 accgctgcgg cggccgaaag ccgccgcctg gaccacgcgc ccaacgcgct cgagcaactg 2340 gccgccgtcg tcgcggatgc gctgtacgcc gcgggcggcg cacagcgagg atccgcggca 2400 ctacggttgg cctccgaccc cgaaggctgg atccggtgtc aactcgacgg cgtgcccacc 2460 gagcagtccc tgcggttcac cgcggccctc gacgagctac tggcgccgct tgccgaaccg 2520 cgctacctca tcggacgcaa gatcctcacg ccgcccgccc ggcccgttgc ccggaggctg 2580 ttcgcggttc gtgccgtcgt cgggctatcg ctgcccggca cggttgcctg gcacgccgtg 2640 ccccgctggt tcgcacgaaa caaggatcgg cggcaacatc tggcacaggc atggcgaaag 2700 cacatcggcc caccccgaca actgccagca gactccccac aagggcaagc catcctcgat 2760 ctgttccgcg gcgataaccc gctctcggtg acaacccagc tgcgcacgac ctggcgg 2817 99 309 DNA Mycobacterium tuberculosis 99 gactgcctcc gtgccaggtt agtctgcgcc cacgataggc attgacaacg cgcgttgtcc 60 acgatttggt ccgccgatat cgcgccgtgt cacccagtgc ctcctccggg tggcaacgag 120 cgtggacgag gactgcagct gcatagcttg gcccgcggtg cgtgcggggg cagggagtcc 180 aatgaaaaat gttgcttaga acgccagaaa gtttttaact agatcaggat tgcttagctg 240 tagactttat ttctcaatga ccacgtaagg attgctgcgg ccagtacaac gtgtacaagg 300 agtcgggct 309 100 310 PRT Mycobacterium tuberculosis 100 Met Ser Phe Leu Thr Val Ala Pro Asp Met Val Thr Ala Ala Ala Gly 1 5 10 15 Asn Leu Glu Ser Val Gly Ser Ala Leu Asn Glu Ala Ala Ala Ala Ala 20 25 30 Ala Pro Ala Thr Val Gly Leu Ala Ala Pro Ala Ala Asp Arg Val Ser 35 40 45 Ala Val Val Ala Ala Met Leu Gly Ala Tyr Ala Arg Asp Phe Gln Gly 50 55 60 Ile Ser Ala Gln Ile Ala Gly Phe His Asn Gln Phe Val Gly Ala Leu 65 70 75 80 Arg Gly Gly Ala Ala Ala Tyr Ala Ser Ala Glu Ala Ala Asn Val Gln 85 90 95 Gln Thr Val Val Asn Ala Val Asn Ala Pro Ala Gln Ala Leu Leu Gly 100 105 110 His Pro Leu Ile Gly Pro Glu Thr Val Gly Ser Ser Ala Ala Ala Val 115 120 125 Ser Phe Gly Phe Gly Pro Leu Leu Leu Ala Gly Ser Asp Pro Leu Leu 130 135 140 Ala Val Pro Phe Ser Tyr Pro Ala Ser Leu Pro Thr Pro Phe Gly Pro 145 150 155 160 Val Thr Met Thr Leu Asn Gly Ser Phe Asp Pro Leu Thr Gln Gln Val 165 170 175 Val Phe Asp Ser Gly Ser Leu Thr Ala Pro Ala Pro Phe Val Tyr Gly 180 185 190 Leu Gly Ala Val Gly Pro Ala Leu Thr Thr Met Thr Ala Leu Gln Asn 195 200 205 Ser Gly Thr Ala Phe Ser Gly Ala Val Gln Ser Gly Asn Leu Leu Gly 210 215 220 Ala Ala Gly Ala Leu Leu Gln Ala Pro Gly Asn Ala Val Thr Gly Phe 225 230 235 240 Leu Phe Gly Gln Thr Ala Ile Ser Gln Ser Ile Pro Gly Pro Ser Asn 245 250 255 Leu Gly Tyr Glu Ser Val Gly Ile Ser Val Pro Val Gly Gly Leu Leu 260 265 270 Ala Pro Leu Gln Pro Val Thr Val Thr Leu Thr Pro Thr Ser Gly Met 275 280 285 Pro Thr Ala Ile Gln Leu Ser Gly Thr Gln Phe Gly Gly Leu Leu Pro 290 295 300 Ala Leu Leu Asn Gly Phe 305 310 101 930 DNA Mycobacterium tuberculosis 101 atgtcgtttc tcaccgtggc gccggacatg gtaacggcgg ccgccgggaa tttggaaagc 60 gttggctcgg cactgaatga ggccgctgcg gcggcggcgc cagccacggt tgggctggcg 120 gccccggccg cggatcgggt gtcggcggtc gtcgcggcga tgttgggggc atatgcccgg 180 gattttcaag gcatcagtgc tcagatcgcg ggttttcata accagttcgt gggcgcgttg 240 cggggcggtg cggccgccta cgccagcgcc gaagccgcca acgtccagca gaccgtggtg 300 aacgccgtga atgcgcccgc ccaggcgctg ttggggcacc cgttgatcgg gcccgagacg 360 gtcggctcca gcgccgccgc ggtctccttc ggcttcggcc cgttgctcct cgctggtagc 420 gatccgctgc tggccgtgcc attcagctat ccggccagtc tgcccacccc attcggtcca 480 gtaacgatga cgctcaacgg gtcgtttgat ccgcttaccc aacaggttgt tttcgactcg 540 ggatcactca ccgcgcccgc tccgttcgtg tacggtcttg gtgcggtagg tccagctctc 600 accaccatga ccgcgctgca aaacagcggc acagcatttt ccggcgcggt gcaaagcggg 660 aacctgctag gggccgcggg cgcgcttctg caagctcccg gcaacgcggt gaccggcttc 720 ctgtttggcc aaacagcgat atcgcagtcg ataccggggc catcgaatct gggctacgag 780 tcggtgggta tcagcgttcc ggtcgggggg ctcttggctc cgctgcagcc cgtgacggtc 840 acgttgacgc ccacatctgg tatgccgact gccattcaat tgagtggtac gcagtttggc 900 ggccttcttc ccgccctact caacggtttc 930 102 490 DNA Mycobacterium tuberculosis 102 cgcccgcata cgtccaccat acgttcgggc gactgcccgg gcagtttgcc taccgacgcg 60 gcagccacag atatagggtc catgacgccg cgacgatcgc gaacatgacc agctgagcgg 120 cggccaccca accggcggga tagatcacgc cggtgatgta gtgagcgaca aatccgtccg 180 gtgacagagg tgtcatcgcg gccttggtgc gagcccagcg ctccacccag gtcagcgggc 240 agtcgacccg cttagcggcg atgccgatcc cccatatcac cgccggaaca tgcagccaca 300 tcgtgcgtcg ccaccgcagg gcaaggaaac cgccggcaag gacgtaagcg atgaaagcga 360 agtgcattac caccgttgat acaacgacgg tttcgtacat ctctcgggtt gcctttccag 420 gtcgcggcgc tccggccact gacagaaaag gttcaattcg ccagcgaaaa cccgtcccat 480 gcgatccggc 490 103 324 PRT Mycobacterium tuberculosis 103 Val Ala Leu Val Ser Thr Ala Arg Val Asp Leu Val Cys Glu Gly Gly 1 5 10 15 Gly Val Arg Gly Ile Gly Leu Val Gly Ala Val Asp Ala Leu Ala Asp 20 25 30 Ala Gly Tyr Arg Phe Pro Arg Val Ala Gly Ser Ser Ala Gly Ala Ile 35 40 45 Val Ala Ser Leu Val Ala Ala Leu Gln Thr Ala Gly Glu Pro Val Thr 50 55 60 Arg Leu Ala Glu Met Met Arg Ser Ile Asp Tyr Pro Lys Phe Leu Asp 65 70 75 80 Arg Asn Leu Ile Gly His Val Pro Leu Ile Gly Gly Gly Leu Ser Leu 85 90 95 Leu Leu Ser Asp Gly Val Tyr Arg Gly Ala Tyr Leu Glu Gln Leu Leu 100 105 110 Gly Gly Leu Leu Ala Asp Leu Gly Val His Thr Phe Gly Asp Leu Arg 115 120 125 Thr Gly Glu Ala Pro Glu Gln Phe Ala Trp Ser Leu Val Val Thr Ala 130 135 140 Ser Asp Leu Ser Arg Arg Arg Leu Val Arg Ile Pro Trp Asp Leu Asp 145 150 155 160 Ser Tyr Gly Ile His Pro Asp Asp Phe Ser Val Ala Arg Ala Val His 165 170 175 Ala Ser Ser Ala Ile Pro Phe Val Phe Glu Pro Val Arg Val Arg Gly 180 185 190 Ala Thr Trp Val Asp Gly Gly Leu Leu Ser Asn Phe Pro Val Ala Leu 195 200 205 Phe Asp Arg Thr Asp Ala Glu Pro Arg Trp Pro Thr Phe Gly Ile Arg 210 215 220 Leu Ser Ala Arg Pro Gly Ile Pro Pro Thr Arg Pro Val Gln Gly Pro 225 230 235 240 Val Ser Leu Gly Ile Ala Ala Ile Glu Thr Leu Val Ser Asn Gln Asp 245 250 255 Asn Ala Tyr Ile Asp Asp Pro Cys Thr Val Arg Arg Thr Ile Phe Val 260 265 270 Pro Ala His Asp Val Ser Pro Ile Asp Phe Asp Ile Thr Ala Glu Gln 275 280 285 Arg Glu Ala Leu Tyr Gln Arg Gly Phe Gln Ala Gly Gln Lys Phe Leu 290 295 300 Ala Asn Trp Asn Tyr Ala Asp Cys Leu Ala Asp Cys Gly Gly Pro Phe 305 310 315 320 Thr Pro Ser Leu 104 972 DNA Mycobacterium tuberculosis 104 gtggcgctgg tgagcacagc acgcgtcgac ctggtgtgtg aaggcggcgg ggtccggggg 60 atagggttgg ttggagcggt ggacgcgctg gccgatgccg gttaccgatt tcccagggtg 120 gcgggcagca gcgcgggtgc gatcgtcgcg tcgctggtcg cggccctaca aacggccggt 180 gagccggtga cgcggcttgc cgagatgatg cgcagcatcg actacccgaa gttcctcgac 240 cgcaatctga taggacacgt gccgttgatc ggcgggggac tttctctgct gttgtcggac 300 ggcgtttacc gcggggccta tctggaacag ctgctcggcg gtttgctcgc tgacctaggc 360 gtgcacacct ttggcgactt gcgcaccggc gaggcacccg aacagttcgc ctggtcgctg 420 gtggtcaccg ccagcgacct atcccgtcgc cgactcgttc gcatcccgtg ggacctggac 480 tcctacggca tccacccgga cgacttctcg gtggcgcgtg cggtgcacgc ctcatcggcg 540 atcccgtttg tgttcgagcc tgttcgggtg cgcggcgcta cctgggtcga cggtggcttg 600 ctgtcgaact ttccggtggc gctgttcgac cgaaccgacg ctgaaccgcg atggcccacg 660 ttcgggatca ggttgtcagc gcgtccgggc attccaccta cccggccggt ccaagggcca 720 gtgtcgttgg gcatcgcggc gatcgaaaca ctggtgagca atcaggacaa cgcctacatc 780 gacgatccgt gtaccgttcg gcgcaccatc ttcgtgcccg cccacgacgt gagtccgatc 840 gacttcgaca tcaccgccga acaacgcgag gctctttacc aacgcggatt tcaggcgggt 900 caaaagttct tggcgaactg gaattacgcc gattgtctgg ctgactgcgg cggcccgttc 960 acgccgtcgc tg 972 105 357 PRT Mycobacterium tuberculosis 105 Met Ala Ser Val Ser Phe Glu Gln Ala Thr Arg Arg Tyr Pro Gly Thr 1 5 10 15 Asp Arg Pro Ala Leu Asp Arg Leu Asp Leu Ile Val Gly Asp Gly Glu 20 25 30 Phe Val Val Leu Val Gly Pro Ser Gly Cys Gly Lys Thr Thr Ser Leu 35 40 45 Arg Met Val Ala Gly Leu Glu Thr Leu Asp Cys Gly Arg Ile Arg Ile 50 55 60 Gly Glu Arg Asp Val Thr Glu Val Asp Pro Lys Asp Arg Asp Val Ala 65 70 75 80 Met Val Phe Gln Asn Tyr Ala Leu Tyr Pro His Met Thr Val Ala Gln 85 90 95 Asn Met Gly Phe Ala Leu Lys Val Ala Lys Ile Gly Lys Ala Glu Ile 100 105 110 Arg Glu Arg Val Leu Ala Ala Ala Lys Leu Leu Asp Leu Gln Ser Tyr 115 120 125 Leu Asp Arg Lys Pro Lys Asp Leu Ser Gly Gly Gln Arg Gln Arg Val 130 135 140 Ala Met Gly Arg Ala Ile Val Arg Arg Pro Gln Val Phe Leu Met Asp 145 150 155 160 Glu Pro Leu Ser Asn Leu Asp Ala Lys Leu Arg Gly Gln Thr Arg Asn 165 170 175 Gln Ile Ala Ala Leu Gln Arg Gln Leu Gly Thr Thr Thr Val Tyr Val 180 185 190 Thr His Asp Gln Val Glu Ala Met Thr Met Gly Asp Arg Val Ala Val 195 200 205 Leu Ser Asp Gly Val Leu Gln Gln Cys Ala Ser Pro Arg Glu Leu Tyr 210 215 220 Arg Asn Pro Gly Asn Val Phe Val Ala Gly Phe Ile Gly Ser Pro Ala 225 230 235 240 Met Asn Leu Phe Arg Leu Ser Ile Ala Asp Ser Thr Val Ser Leu Gly 245 250 255 Asp Trp Gln Ile Leu Leu Pro Arg Ala Val Val Gly Thr Ala Ala Glu 260 265 270 Val Ile Ile Gly Val Arg Pro Glu His Leu Glu Leu Gly Gly Ala Gly 275 280 285 Ile Glu Met Asp Val Asp Met Val Glu Glu Leu Gly Ala Asp Ala Tyr 290 295 300 Leu Tyr Gly Arg Ile Val Ser Gly Gly Cys Glu Met Asp Gln Ser Ile 305 310 315 320 Val Ala Arg Val Asp Gly Arg Gly Pro Pro Glu Arg Gly Ser Arg Val 325 330 335 Arg Leu Cys Pro Thr Pro Gly His Leu His Phe Phe Ala Val Asp Gly 340 345 350 Arg Arg Ile Pro Gly 355 106 1071 DNA Mycobacterium tuberculosis 106 atggcttcgg tgagttttga gcaggcaacc cggcgctatc ccggcacgga ccgaccggcc 60 ctggatcggc tcgacctgat cgtcggcgat ggcgagttcg ttgtcctggt ggggccgtcc 120 ggatgtggca agacgacgtc gttacggatg gtggctggct tggagacgct ggactgtggg 180 cgtatccgga tcggcgagcg cgacgtcacc gaggtcgatc ccaaggatcg tgatgtcgcc 240 atggtgttcc agaactacgc cctctacccg cacatgacgg tggcgcagaa catgggcttc 300 gcgttgaagg tcgccaagat cggcaaggcc gagatccgcg agcgggtgct tgccgcagcg 360 aaattgcttg atctgcaatc ttatctggat cgcaagccga aagatctctc cggcggccaa 420 cggcaacggg tggcgatggg tcgtgcgatc gtgcggcgcc cacaggtatt cctgatggac 480 gaaccgctgt ccaatcttga cgccaaactt cgcgggcaaa cccgcaatca gatcgccgcg 540 ttacaacggc aactgggtac gaccaccgtg tatgtcactc acgaccaggt cgaggccatg 600 acgatgggtg accgcgtcgc ggtgctgtct gacggtgtgc tgcaacagtg tgcttcgcct 660 cgagagctct accgcaaccc gggcaacgtg ttcgtcgcgg ggttcatcgg ttccccggcg 720 atgaacctgt tcaggctttc catcgccgat tccacggtgt cactgggtga ttggcagatc 780 ctgctgccgc gtgcggtcgt cggtacggca gccgaggtca ttatcggtgt tcgccccgaa 840 catttggagc tgggcggcgc cggcatcgag atggacgtcg acatggtcga agaacttgga 900 gcggacgcct acttgtatgg ccgaatcgtg tcgggcggct gcgaaatgga ccagtcaatc 960 gtcgctcgag tggacggccg cggcccgccc gagcggggta gtcgcgtgcg gctatgtccc 1020 acaccgggac acctgcactt cttcgccgtc gacgggcgtc ggattccggg c 1071 107 280 PRT Mycobacterium tuberculosis 107 Val Gly Trp Ala Asp Arg Ile Val His Arg His Phe Ile Arg Gly Leu 1 5 10 15 Ala Leu Tyr Ala Gly Leu Ile Gly Ile Ala Trp Cys Ala Leu Phe Pro 20 25 30 Ile Ile Trp Ala Leu Ser Gly Ser Leu Lys Ala Asp Gly Glu Val Thr 35 40 45 Glu Pro Thr Leu Phe Pro Ser His Pro Gln Trp Ser Asn Tyr Arg Glu 50 55 60 Val Phe Ala Leu Met Pro Phe Trp Arg Met Phe Phe Asn Thr Val Leu 65 70 75 80 Tyr Ala Gly Cys Val Thr Ala Gly Gln Val Phe Phe Cys Ser Leu Ala 85 90 95 Gly Tyr Ala Phe Ala Arg Leu Gln Phe Arg Gly Arg Asp Thr Leu Phe 100 105 110 Val Leu Tyr Leu Ser Thr Leu Met Val Pro Leu Thr Val Thr Val Ile 115 120 125 Pro Gln Val Ile Leu Met Arg Ile Val Gly Trp Val Asp Thr Pro Trp 130 135 140 Ala Met Ile Val Pro Gly Leu Phe Gly Ser Ala Phe Gly Thr Tyr Leu 145 150 155 160 Met Arg Gln Phe Phe Arg Thr Leu Pro Thr Asp Leu Glu Glu Ala Ala 165 170 175 Ile Leu Asp Gly Cys Ser Pro Trp Gln Ile Tyr Trp Arg Ile Leu Leu 180 185 190 Pro His Ser Arg Pro Ala Val Leu Val Leu Gly Val Leu Thr Trp Val 195 200 205 Asn Val Trp Asn Asp Phe Leu Trp Pro Leu Leu Met Ile Gln Arg Asn 210 215 220 Ser Leu Ala Thr Leu Thr Leu Gly Leu Val Arg Leu Arg Gly Glu Tyr 225 230 235 240 Val Ala Arg Trp Pro Val Leu Met Ala Ala Ser Met Leu Met Leu Val 245 250 255 Pro Leu Val Ile Leu Tyr Ala Val Ala Gln Arg Ser Phe Val Arg Gly 260 265 270 Ile Ala Val Thr Gly Leu Gly Gly 275 280 108 840 DNA Mycobacterium tuberculosis 108 gtgggctggg ctgatcgaat agtccaccgc cacttcattc gtgggcttgc cctgtacgcg 60 ggactgatcg ggatcgcttg gtgcgcgctg ttccctatca tctgggcgct gtcgggctcc 120 ctgaaggcgg acggcgaggt gaccgagccg acgctgttcc cgtcgcatcc gcaatggtcc 180 aactaccgcg aggtgttcgc gttgatgccg ttctggcgga tgttcttcaa caccgtgctg 240 tatgccggat gtgtcaccgc cgggcaggtc ttcttctgct cgttggccgg ttatgccttc 300 gcgcgactgc agttccgggg ccgcgatacg ttgttcgtct tgtacttgag cactttgatg 360 gtgccgttga cggtgaccgt catcccacag gtcattctca tgcggatcgt ggggtgggtg 420 gatacgccgt gggcgatgat cgtgccggga ttgttcggta gcgcgttcgg tacctacctg 480 atgcggcagt tcttccgcac gctgccgacc gatctcgagg aagccgcgat tctcgacggt 540 tgctcgccgt ggcagatcta ctggcggatt ctgctgccgc attcacgtcc cgcggtgctg 600 gtgctgggtg tgctcacctg ggtcaacgtg tggaacgact ttctgtggcc gctgctgatg 660 atccagcgaa acagcctggc gacgctcacc cttggcctgg tccgattgcg gggcgaatac 720 gtcgcccggt ggccggtgct gatggcggcg tcgatgctga tgctggtgcc gttggtcatc 780 ctttatgcgg tcgcacaacg ttcctttgtc cgtggtatcg cggtgactgg gctcggcggg 840 109 300 PRT Mycobacterium tuberculosis 109 Met Thr Arg Arg Arg Gly Arg Arg Ala Trp Ala Gly Arg Met Phe Val 1 5 10 15 Ala Pro Asn Leu Ala Ala Val Val Val Phe Met Leu Phe Pro Leu Gly 20 25 30 Phe Ser Leu Tyr Met Ser Phe Gln Lys Trp Asp Leu Phe Thr His Ala 35 40 45 Thr Phe Val Arg Leu Asp Asn Phe Arg Asn Leu Phe Thr Ser Asp Pro 50 55 60 Leu Phe Leu Ile Ala Val Val Asn Thr Ala Val Tyr Thr Val Gly Thr 65 70 75 80 Val Val Pro Thr Val Ile Val Ser Leu Val Val Ala Ala Phe Leu Asn 85 90 95 Arg Lys Ile Lys Gly Ile Ser Leu Phe Arg Thr Val Val Phe Leu Pro 100 105 110 Leu Ala Ile Ser Ser Val Val Met Ala Val Val Trp Gln Phe Val Phe 115 120 125 Asn Thr Asp Asn Gly Leu Leu Asn Ile Met Leu Gly Trp Leu Gly Ile 130 135 140 Gly Pro Ile Pro Trp Leu Ile Glu Pro Arg Trp Ala Met Val Ser Leu 145 150 155 160 Cys Leu Val Ser Val Trp Arg Ser Val Pro Phe Ala Thr Val Val Leu 165 170 175 Leu Ala Ala Met Gln Gly Val Pro Glu Thr Val Tyr Glu Ala Ala Arg 180 185 190 Ile Asp Gly Ala Gly Glu Ile Arg Gln Phe Val Ser Ile Thr Val Pro 195 200 205 Leu Ile Arg Gly Ala Leu Ser Phe Val Val Val Ile Ser Ile Ile His 210 215 220 Ala Phe Gln Ala Phe Asp Leu Val Tyr Val Leu Thr Gly Ala Asn Gly 225 230 235 240 Gly Pro Glu Thr Ala Thr Tyr Val Leu Gly Ile Met Leu Phe Gln His 245 250 255 Ala Phe Ser Phe Leu Glu Phe Gly Tyr Ala Ser Ala Leu Ala Trp Val 260 265 270 Met Phe Ala Ile Leu Leu Val Leu Thr Val Leu Gln Leu Arg Ile Thr 275 280 285 His Arg Arg Ser Trp Glu Ala Ser Arg Gly Leu Gly 290 295 300 110 900 DNA Mycobacterium tuberculosis 110 atgacacggc gcagggggcg acgcgcgtgg gcggggcgta tgttcgtcgc gccgaacttg 60 gctgccgttg tggtgttcat gctgtttccg ctgggattct cgctgtacat gagctttcag 120 aagtgggact tgtttacgca tgcgacgttc gtgaggttgg acaatttcag aaacctcttc 180 acttctgatc cgctgtttct catcgccgtg gtcaacaccg cggtttacac cgtcggcacc 240 gtggtaccga ccgttatcgt cagcctcgtc gtcgccgcct ttctaaaccg gaaaatcaaa 300 ggcatcagcc tctttcggac ggtcgtcttc ttgccgttgg cgatttcctc ggtggtgatg 360 gcggtcgtct ggcagttcgt cttcaacacc gacaatggcc tactcaacat catgctcggc 420 tggctgggaa tcggccccat cccatggcta atcgaacccc gatgggccat ggtctcgctt 480 tgcctggtca gcgtctggcg cagtgtgccc ttcgccacgg tcgtcctgct ggccgcgatg 540 cagggggttc cggagactgt gtacgaggcg gccaggatcg atggtgccgg cgagattcgc 600 cagttcgtgt ccatcacggt accgctgatc cggggggcat tgtcattcgt ggttgtcata 660 tcgatcatcc acgcgttcca ggcgtttgac cttgtctacg tccttaccgg tgccaacggt 720 ggtcccgaga cggctaccta tgttttgggc atcatgctgt tccagcacgc gttttcgttc 780 ctggaattcg gctatgcgtc cgcgttggcg tgggtgatgt tcgccatctt gctggtgttg 840 accgtgctgc agttgcgaat tacgcaccgg cgctcctggg aggcgtcccg tgggctgggc 900 111 439 PRT Mycobacterium tuberculosis 111 Met Val Asn Lys Pro Phe Glu Arg Arg Ser Leu Leu Arg Gly Ala Gly 1 5 10 15 Ala Leu Thr Ala Ala Ser Leu Ala Pro Trp Ala Ala Gly Cys Ala Ala 20 25 30 Asp Asp Asp Asp Ala Leu Thr Phe Phe Phe Ala Ala Asn Pro Asp Glu 35 40 45 Leu Arg Pro Arg Met Arg Val Val Asn Glu Phe Gln Arg Arg Tyr Pro 50 55 60 Asp Ile Lys Val Arg Ala Leu Leu Ser Gly Pro Gly Val Met Gln Gln 65 70 75 80 Leu Ala Thr Phe Cys Ala Gly Gly Lys Cys Pro Asp Val Leu Met Ala 85 90 95 Trp Glu Leu Thr Tyr Ala Glu Leu Ala Asp Arg Gly Val Leu Leu Asp 100 105 110 Leu Asn Thr Leu Leu Ala Arg Asp Gln Ala Phe Ala Ala Glu Leu Lys 115 120 125 Ser Asp Ser Ile Gly Ala Leu Tyr Glu Thr Phe Thr Phe Asn Gly Gly 130 135 140 Gln Tyr Ala Phe Pro Glu Gln Trp Ser Gly Asn Phe Leu Phe Tyr Asn 145 150 155 160 Lys Gln Leu Phe Asp Asp Ala Gly Val Pro Pro Pro Pro Gly Ser Trp 165 170 175 Glu Arg Pro Trp Ser Phe Ala Glu Phe Leu Asp Ala Ala Gln Ala Leu 180 185 190 Thr Lys Gln Gly Arg Ser Gly Arg Asp Arg Gln Trp Gly Phe Val Asn 195 200 205 Ala Trp Val Ser Phe Tyr Ala Ala Gly Leu Phe Ala Met Asn Asn Gly 210 215 220 Val Pro Trp Ser Val Pro Arg Met Asn Pro Thr His Leu Asn Phe Asp 225 230 235 240 His Asp Gly Phe Leu Glu Ala Val Gln Phe Tyr Ala Asp Leu Thr Asn 245 250 255 Lys His Lys Val Ala Pro Ser Ala Ala Glu Gln Gln Ser Met Ser Thr 260 265 270 Ala Asp Leu Phe Ser Val Gly Lys Ala Gly Ile Ala Leu Ala Gly His 275 280 285 Trp Arg Tyr Gln Thr Phe Asp Arg Ala Asp Gly Leu Asp Phe Asp Val 290 295 300 Ala Pro Leu Pro Ile Gly Pro Arg Gly Arg Ala Ala Cys Ser Asp Ile 305 310 315 320 Gly Val Thr Gly Leu Ala Ile Ala Ala Thr Ser Arg Arg Lys Asp Gln 325 330 335 Ala Trp Glu Phe Val Lys Phe Ala Thr Gly Pro Val Gly Gln Ala Leu 340 345 350 Ile Gly Glu Ser Arg Leu Phe Val Pro Val Leu Arg Ser Ala Ile Asn 355 360 365 Ser His Gly Phe Ala Asn Ala His Arg Arg Val Gly Asn Leu Ala Val 370 375 380 Leu Ser Glu Gly Pro Ala Tyr Ser Glu Gly Leu Pro Val Thr Pro Ala 385 390 395 400 Trp Glu Lys Ile Ala Ala Leu Met Asp Arg Tyr Phe Gly Pro Val Leu 405 410 415 Arg Gly Ser Arg Pro Ala Thr Ser Leu Thr Gly Leu Ser Gln Ala Val 420 425 430 Asp Glu Val Leu Arg Asn Pro 435 112 1317 DNA Mycobacterium tuberculosis 112 atggtcaata agccgttcga gcggcgcagt ctgttacggg gtgcgggcgc gcttactgcg 60 gcctcgctgg ctccctgggc cgctgggtgt gctgccgatg acgatgacgc gttgactttc 120 ttttttgcag ccaatccgga cgagctccgt ccccggatgc gcgtcgtcaa cgaattccag 180 cggcgctatc ccgatatcaa ggtacgggcc ctgttgtccg gacccggcgt catgcagcag 240 ctcgcaacgt tttgcgcggg tggcaagtgt ccggatgtgc tgatggcatg ggaactgacc 300 tatgccgaac tggccgaccg gggggtgttg cttgacctga acacgctatt ggcgcgcgac 360 caggctttcg ccgcggagct gaaatcggac agcatcgggg ccctgtatga gactttcacg 420 ttcaacggag gccagtacgc ctttccggag caatggtccg gcaacttctt gttctacaac 480 aaacagctat tcgacgacgc cggcgtgcca ccgccgcccg gtagctggga acggccatgg 540 agcttcgccg aattcctgga tgccgcccag gcgcttacca agcagggccg gtcgggacgg 600 gacaggcaat ggggcttcgt caacgcgtgg gtctcgttct acgctgccgg gttgttcgcc 660 atgaataacg gtgtaccgtg gtcggttccg cggatgaatc ccacccacct caatttcgac 720 cacgatgggt tcctcgaagc ggtgcagttc tacgccgacc tgaccaacaa gcacaaggtg 780 gcccccagcg ctgctgagca gcagtcgatg tcgacggcgg acctgttttc tgtgggcaag 840 gccgggatcg cgttggccgg gcactggcga tatcagacgt tcgaccgtgc cgacggtctg 900 gacttcgacg tcgccccact gcccatcggt ccgcgcggac gagccgcctg ttcagatatc 960 ggtgtcaccg ggctggccat tgcggcgacc agtcgacgca aggaccaggc gtgggaattc 1020 gtaaagttcg cgaccggccc ggtggggcag gcattgatcg gcgaatcccg cctgttcgtg 1080 ccggtgctga gatcggcgat caactcgcac ggattcgcca acgcccaccg cagggtaggc 1140 aatcttgccg tgctcagcga ggggccggcc tattcggaag gcttgccggt gaccccggcc 1200 tgggagaaga tcgccgccct gatggaccgc tacttcggac ccgtgctgcg tggatcccgg 1260 ccggcgacct cgctgaccgg gctatcacag gccgtcgatg aagtgctgcg caatcca 1317 113 265 PRT Mycobacterium tuberculosis 113 Met Ala Pro Pro Asn Arg Asp Glu Leu Leu Ala Ala Val Glu Arg Ser 1 5 10 15 Pro Gln Ala Ala Ala Ala His Asp Arg Ala Gly Trp Val Gly Leu Phe 20 25 30 Thr Gly Asp Ala Arg Val Glu Asp Pro Val Gly Ser Gln Pro Gln Val 35 40 45 Gly His Glu Ala Ile Gly Arg Phe Tyr Asp Thr Phe Ile Gly Pro Arg 50 55 60 Asp Ile Thr Phe His Arg Asp Leu Asp Ile Val Ser Gly Thr Val Val 65 70 75 80 Leu Arg Asp Leu Glu Leu Glu Val Ala Met Asp Ser Ala Val Thr Val 85 90 95 Phe Ile Pro Ala Phe Leu Arg Tyr Asp Leu Arg Pro Val Thr Gly Glu 100 105 110 Trp Gln Ile Ala Ala Leu Arg Ala Tyr Trp Glu Leu Pro Ala Met Met 115 120 125 Leu Gln Phe Leu Arg Thr Gly Ser Gly Ala Thr Arg Pro Ala Leu Gln 130 135 140 Leu Ser Arg Ala Leu Leu Gly Asn Gln Gly Leu Gly Gly Thr Ala Gly 145 150 155 160 Phe Leu Thr Gly Phe Arg Arg Ala Gly Arg Arg His Lys Lys Leu Val 165 170 175 Glu Thr Phe Leu Asn Ala Ala Ser Arg Ala Asp Lys Ser Ala Ala Tyr 180 185 190 His Ala Leu Ser Arg Thr Ala Thr Met Thr Leu Gly Glu Asp Glu Leu 195 200 205 Leu Asp Ile Val Glu Leu Phe Glu Gln Leu Arg Gly Ala Ser Trp Thr 210 215 220 Lys Val Thr Gly Ala Gly Ser Thr Val Ala Val Ser Leu Ala Ser Asp 225 230 235 240 His Arg Arg Gly Ile Met Phe Ala Asp Val Pro Trp Arg Gly Asn Arg 245 250 255 Ile Asn Arg Ile Arg Tyr Phe Pro Ala 260 265 114 795 DNA Mycobacterium tuberculosis 114 atggcaccgc cgaaccggga tgaactgttg gcggcggtgg agcgctcgcc gcaagcggcc 60 gccgcgcacg accgcgccgg ctgggtcggg ttgttcaccg gtgacgcgcg ggtcgaagac 120 ccggtgggtt cgcagccgca ggtggggcat gaggccatcg gccgcttcta cgacaccttc 180 atcgggccgc gggatatcac gttccatcgc gatctggata tcgtctccgg cacggtggtg 240 ctgcgcgatc tcgaactcga ggtcgcgatg gactcggctg tgacggtgtt cattcccgcc 300 ttcctacgct atgacctacg accggttacc ggcgagtggc agattgccgc actgcgggcg 360 tactgggagt tgccggcgat gatgctgcag tttctgcgca cgggatcggg ggccacaaga 420 cccgccctgc aactgtcgcg agcgctgcta ggcaatcaag ggttgggcgg caccgcagga 480 ttcctgaccg gctttcgccg ggcgggccgg cggcacaaga agctggtgga aacgttcctc 540 aacgccgcgt cccgggcaga caagtccgct gcgtatcacg cgttatcacg cactgccaca 600 atgactttag gcgaggatga gctactcgac attgtcgagc tgttcgagca gctgcgcggg 660 gctagctgga ccaaggtgac cggtgccgga tccaccgtcg cggtgtcgct cgcgtcggac 720 caccggcgcg gcatcatgtt cgccgacgtg ccgtggcgcg gcaaccggat caatcggatt 780 cggtacttcc cagcc 795 115 186 PRT Mycobacterium tuberculosis 115 Met Arg Ala Leu Ile Ile Val Asp Val Gln Asn Asp Phe Cys Glu Gly 1 5 10 15 Gly Ser Leu Ala Val Thr Gly Gly Ala Ala Leu Ala Arg Ala Ile Ser 20 25 30 Asp Tyr Leu Ala Glu Ala Ala Asp Tyr His His Val Val Ala Thr Lys 35 40 45 Asp Phe His Ile Asp Pro Gly Asp His Phe Ser Gly Thr Pro Asp Tyr 50 55 60 Ser Ser Ser Trp Pro Pro His Cys Val Ser Gly Thr Pro Gly Ala Asp 65 70 75 80 Phe His Pro Ser Leu Asp Thr Ser Ala Ile Glu Ala Val Phe Tyr Lys 85 90 95 Gly Ala Tyr Thr Gly Ala Tyr Ser Gly Phe Glu Gly Val Asp Glu Asn 100 105 110 Gly Thr Pro Leu Leu Asn Trp Leu Arg Gln Arg Gly Val Asp Glu Val 115 120 125 Asp Val Val Gly Ile Ala Thr Asp His Cys Val Arg Gln Thr Ala Glu 130 135 140 Asp Ala Val Arg Asn Gly Leu Ala Thr Arg Val Leu Val Asp Leu Thr 145 150 155 160 Ala Gly Val Ser Ala Asp Thr Thr Val Ala Ala Leu Glu Glu Met Arg 165 170 175 Thr Ala Ser Val Glu Leu Val Cys Ser Ser 180 185 116 558 DNA Mycobacterium tuberculosis 116 atgcgggcgt tgatcatcgt cgacgtgcag aacgacttct gcgagggtgg ctcgctggcg 60 gtaaccggtg gcgccgcgct ggcccgcgcc atcagcgact acctggccga agcggcggac 120 taccatcacg tcgtggcaac caaggacttc cacatcgacc cgggtgacca cttctccggc 180 acaccggact attcctcgtc gtggccaccg cattgcgtca gcggtactcc cggcgcggac 240 ttccatccca gtctggacac gtcggcaatc gaggcggtgt tctacaaggg tgcctacacc 300 ggagcgtaca gcggcttcga aggagtcgac gagaacggca cgccactgct gaattggctg 360 cggcaacgcg gcgtcgatga ggtcgatgtg gtcggtattg ccaccgatca ttgtgtgcgc 420 cagacggccg aggacgcggt acgcaatggc ttggccacca gggtgctggt ggacctgaca 480 gcgggtgtgt cggccgatac caccgtcgcc gcgctggagg agatgcgcac cgccagcgtc 540 gagttggttt gcagctcc 558 117 213 PRT Mycobacterium tuberculosis 117 Val Lys Ala Ala Asp Ser Ala Glu Ser Asp Ala Gly Ala Asp Gln Thr 1 5 10 15 Gly Pro Gln Val Lys Ala Ala Asp Ser Ala Glu Ser Asp Ala Gly Glu 20 25 30 Leu Gly Glu Asp Ala Cys Pro Glu Gln Ala Leu Val Glu Arg Arg Pro 35 40 45 Ser Arg Leu Arg Arg Gly Trp Leu Val Gly Ile Ala Ala Thr Leu Leu 50 55 60 Ala Leu Ala Gly Gly Leu Gly Ala Ala Gly Tyr Phe Ala Leu Arg Ser 65 70 75 80 His Gln Glu Ser Gln Ser Ile Ala Arg Glu Asp Leu Ala Ala Ile Glu 85 90 95 Ala Ala Lys Asp Cys Val Ala Ala Thr Gln Ala Pro Asp Ala Gly Ala 100 105 110 Met Ser Ala Ser Met Gln Lys Ile Ile Glu Cys Gly Thr Gly Asp Phe 115 120 125 Gly Ala Gln Ala Ser Leu Tyr Thr Ser Met Leu Val Glu Ala Tyr Gln 130 135 140 Ala Ala Ser Val His Val Gln Val Thr Asp Met Arg Ala Ala Val Glu 145 150 155 160 Arg Asn Asn Asn Asp Gly Ser Val Asp Val Leu Val Ala Leu Arg Val 165 170 175 Lys Val Ser Asn Thr Asp Ser Asp Ala His Glu Val Gly Tyr Arg Leu 180 185 190 Arg Val Arg Met Ala Leu Asp Glu Gly Arg Tyr Lys Ile Ala Lys Leu 195 200 205 Asp Gln Val Thr Lys 210 118 639 DNA Mycobacterium tuberculosis 118 gtgaaggcgg cggattcggc ggaatctgac gccggagccg accagactgg cccgcaggtg 60 aaggcggcgg attcggcgga atctgacgcc ggagagctcg gcgaggacgc gtgcccagaa 120 caggccctcg tcgagcggcg cccgtcgcgg ttgcggcgag gctggcttgt tggcattgcg 180 gcgacgctgc tcgcgttggc cggtggcctt ggcgcagcgg gttattttgc gttgcgctca 240 caccaggaaa gccaatcaat cgcgcgcgag gaccttgcgg ccattgaggc cgctaaggat 300 tgcgttgcgg ccacgcaggc acccgatgct ggggcgatgt cggctagcat gcagaagatc 360 atcgagtgtg gcaccggtga tttcggtgcc caggcgtcgt tgtacaccag catgctcgtc 420 gaggcgtatc aagcggccag cgtccacgtg caagtgaccg atatgcgcgc ggcggtcgag 480 cgcaacaaca atgacgggtc ggtcgatgtt ctggtggcgc tccgggtcaa ggtgtccaac 540 accgactcgg atgcccatga agtcggctac cgtcttcggg tccggatggc actggatgag 600 ggccgctata agatcgccaa actcgaccag gtgacgaag 639 

1. A method of identifying a mycobacterial nucleic acid promoter sequence which is induced or up-regulated during mycobacterial virulence, said method comprising: infecting a macrophage target cell with a Mycobacterium tuberculosis host cell, which host cell contains a nucleic acid construct comprising a putative mycobacterial promoter sequence operably linked to a coding sequence of a reporter gene located down-stream from the promoter; culturing the macrophage under conditions which support mycobacterial virulence; and identifying a promoter sequence which is induced or up-regulated during virulence by detecting expression of the reporter sequence.
 2. A method according to claim 1, wherein the induced or up-regulated promoter sequence is detected by increased expression of the reporter gene under conditions which support mycobacterial virulence when compared with the corresponding level of expression when cultured under conditions which do not promote mycobacterial virulence.
 3. A method according to claim 1 or 2, wherein the putative promoter sequence is derived from M. tuberculosis or M. bovis.
 4. A method according to any preceding claim, wherein the reporter sequence encodes a green fluorescence protein.
 5. A method according to claim 4, wherein a mycobacterial host cell having a promoter induced or up-regulated during mycobacterial virulence is separated from other host cells by fluorescence activated cell sorting.
 6. A method of identifying a mycobacterial gene the expression of which is induced or up-regulated during mycobacterial virulence, said method comprising: identifying a mycobacterial promoter sequence which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell, wherein the host cell contains a nucleic acid construct comprising said promoter sequence operably linked to a coding sequence of a reporter gene located down-stream from the promoter; aligning by sequence homology the nucleic acid sequence of the promoter with published nucleic acid sequence data for the same mycobacterial species; and identifying the associated nucleic acid coding sequence under the control of said promoter.
 7. An isolated mycobacterial promoter obtainable by a method according to any of claims 1-5, wherein the promoter preferably has the nucleic acid sequence of SEQ ID NO: 1; 18; 37; 54; 57; 66; 71; 74; 77; 84; 91; 96; 99; or
 102. 8. An isolated nucleic acid coding sequence obtainable by a method according to claim 6, wherein the coding sequence preferably has the nucleic acid sequence of SEQ ID NO: 3; 5; 7; 9; 11; 13; 15; 17; 20; 22; 24; 26; 28; 30; 32; 34; 36; 39; 41; 43; 45; 47; 49; 51; 53; 56; 59; 61; 63; 65; 68; 70; 73; 76; 79; 81; 83; 86; 88; 90; 93; 95; 98; 101; 104; 106; 108; 110; 112; 114; 116; or
 118. 9. An isolated mycobacterial peptide or a fragment or derivative or variant thereof, wherein the peptide is encoded by a mycobacterial gene the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene.
 10. A pharmaceutical composition comprising a peptide, or a fragment or variant or derivative thereof, wherein the peptide is selected from the group consisting of SEQ ID NO: 2; 4; 6; 8; 10; 12; 14; 16; 19; 21; 23; 25; 27; 29; 31; 33; 35; 38; 40; 42; 44; 46; 48; 50; 52; 55; 58; 60; 62; 64; 67; 69; 72; 75; 78; 80; 82; 85; 87; 89; 92; 94; 97; 100; 103; 105; 107; 109; 111; 113; 115; and
 117. 11. An inhibitor of a mycobacterial peptide, wherein the peptide is encoded by a mycobacterial gene the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, and wherein the inhibitor is capable of substantially preventing or inhibiting the mycobacterial peptide from exerting its native biological function or effect.
 12. An inhibitor according to claim 11, selected from the group consisting of: an antibiotic capable of targeting the induced or up-regulated mycobacterial gene, or the gene product thereof; and an antisense or triplex-forming nucleic acid sequence which is complementary to at least part of the inducible or up-regulatable gene.
 13. An antibody which binds to a peptide encoded by a gene, or to a fragment or variant or derivative of said peptide, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene.
 14. An antibody according to claim 13, wherein the peptide is selected from the group consisting of SEQ ID NO: 2; 4; 6; 8; 10; 12; 14; 16; 19; 21; 23; 25; 27; 29; 31; 33; 35; 38; 40; 42; 44; 46; 48; 50; 52; 55; 58; 60; 62; 64; 67; 69; 72; 75; 78; 80; 82; 85; 87; 89; 92; 94; 97; 100; 103; 105; 107; 109; 111; 113; 115; and
 117. 15. An attenuated mycobacterium in which a gene has been modified, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, thereby rendering the mycobacterium substantially non-pathogenic.
 16. An attenuated mycobacterium according to claim 15, wherein the gene to be modified has a wild-type coding sequence corresponding to one of the group consisting of SEQ ID NO: 3; 5; 7; 9; 11; 13; 15; 17; 20; 22; 24; 26; 28; 30; 32; 34; 36; 39; 41; 43; 45; 47; 49; 51; 53; 56; 59; 61; 63; 65; 68; 70; 73; 76; 79; 81; 83; 86; 88; 90; 93; 95; 98; 101; 104; 106; 108; 110; 112; 114; 116; and
 118. 17. An attenuated microbial carrier, comprising a peptide encoded by a gene, or a fragment or variant or derivative of said peptide, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene.
 18. An attenuated microbial carrier according to claim 17, wherein the peptide is selected from the group consisting of SEQ ID NO: 2; 4; 6; 8; 10; 12; 14; 16; 19; 21; 23; 25; 27; 29; 31; 33; 35; 38; 40; 42; 44; 46; 48; 50; 52; 55;. 58; 60; 62; 64; 67; 69; 72; 75; 78; 80; 82; 85; 87; 89; 92; 94; 97; 100; 103; 105; 107; 109; 111; 113; 115; and
 117. 19. An attenuated microbial carrier according to claim 17 or 18, wherein the attenuated microbial carrier is attenuated salmonella, attenuated vaccinia virus, attenuated fowipox virus, or attenuated M. bovis (eg. BCG strain).
 20. A DNA plasmid comprising a promoter, a polyadenylation signal, and a DNA sequence which corresponds to the coding sequence of a mycobacterial gene, or a fragment or variant or derivative of said DNA sequence, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, wherein the promoter and polyadenylation signal are operably linked to the DNA sequence.
 21. A DNA plasmid according to claim 20, wherein the coding sequence of said gene is selected from the group consisting of SEQ ID NO: 3; 5; 7; 9; 11; 13; 15; 17; 20; 22; 24; 26; 28; 30; 32; 34; 36; 39; 41; 43; 45; 47; 49; 51; 53; 56; 59; 61; 63; 65; 68; 70; 73; 76; 79; 81; 83; 86; 88; 90; 93; 95; 98; 101; 104; 106; 108; 110; 112; 114; 116; and
 118. 22. A DNA plasmid according to claim 20 or 21, wherein the promoter is selected from the group consisting of: CMV; and SV40 promoters; and the polyadenylation signal is selected from the group consisting of: SV40; and bovine growth hormone polyadenylation signals.
 23. An isolated RNA sequence which is encoded by the coding sequence of a mycobacterial gene, or a fragment or variant or derivative of said coding sequence, the expression of which gene is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene.
 24. An RNA vector comprising the RNA sequence of claim 23 and an integration site for a chromosome of a host cell.
 25. Use of a peptide or fragment or variant or derivative according to claim 9 or claim 10, an inhibitor according to claim 11 or claim 12, an antibody according to claim 13 or claim 14, an attenuated mycobacterium according to claim 15 or claim 16, an attenuated microbial carrier according to any of claims 17-19, a DNA sequence corresponding to the coding sequence of a gene which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, or a fragment or variant or derivative of said DNA sequence, a DNA plasmid according to any of claims 20-22, an RNA sequence according to claim 23, and/or an RNA vector according to claim 24, in the manufacture of a medicament for treating or preventing a mycobacterial infection.
 26. A method of treating or preventing a mycobacterial infection, by administering to a patient a peptide or fragment or variant or derivative according to claim 9 or claim 10, an inhibitor according to claim 11 or claim 12, an antibody according to claim 13 or claim 14, an attenuated mycobacterium according to claim 15 or claim 16, an attenuated microbial carrier according to any of claims 17-19, a DNA sequence corresponding to the coding sequence of a gene which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, or a fragment or variant or derivative of said DNA sequence, a DNA plasmid according to any of claims 20-22, an RNA sequence according to claim 23, and/or an RNA vector according to claim
 24. 27. Use of a peptide or fragment or variant or derivative according to claim 9 or claim 10, or an antibody according to claim 13 or claim 14, or a polynucleotide probe comprising at least 8 nucleotides wherein said probe binds to at least part of a gene which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, in the manufacture of a diagnostic reagent for identifying a mycobacterial infection.
 28. A recombinant method of preparing a mycobacterial peptide, or a fragment or derivative or a variant of said peptide, wherein the peptide is encoded by a mycobacterial gene the expression of which is induced or up-regulated during infection of a macrophage by a M. tuberculosis host cell containing said gene, comprising expressing a nucleic acid sequence corresponding to the coding sequence of said gene, or a fragment or variant or derivative of said nucleic acid sequence, in a host cell.
 29. An isolated peptide, an inhibitor, an antibody, an attenuated mycobacterium, an attenuated microbial carrier, an isolated RNA molecule, an RNA vector, or a DNA plasmid substantially as hereinbefore described with reference to the Examples. 